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    <!-- http://purl.obolibrary.org/obo/GENO_0000481 -->

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        <rdfs:label xml:lang="en">genomic feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/GENO_0000512 -->

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        <rdfs:label>allele</rdfs:label>
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        <ns3:IAO_0000116>A landsacpe review found mostly gene-centric definitions of &#39;allele&#39; that represented a particular version of a gene, or variation within a gene sequence [1][2][3][4][5][6][6a].  But we also found &#39;allele&#39; used to refer to other types and extents of variation - including single nucleotide polymorphisms, repeat regions, and copy number variations [7][8][9][10][11], where such variations don&#39;t neccessarily impact a gene.

To be maximally accommodating of how this term is used across research communities, GENO defines &#39;allele&#39; broadly and allow alleles can span any locus or extent of sequence. While &#39;alleles&#39; encountered in public datases typically overlap a gene, many do not. But GENO does define the &#39;gene allele&#39; class as a subtype of &#39;allele&#39; to refers more specifically to a specifc version of an entire gene.
	
[1] https://isogg.org/wiki/Allele (retrieved 2018-03-17)
[2] http://semanticscience.org/resource/allele (retrieved 2018-03-17)
[3] https://en.wikipedia.org/wiki/Allele (retrieved 2018-03-17)
[4] https://www.cancer.gov/publications/dictionaries/genetics-dictionary/def/allele (retrieved 2018-03-17)
[5] http://purl.obolibrary.org/obo/SO_0001023 (retrieved 2018-03-17)
[6] http://purl.obolibrary.org/obo/NCIT_C16277 (retrieved 2018-03-17)
[6a] https://www.ncbi.nlm.nih.gov/mesh/68000483
[7] https://www.snpedia.com/index.php/Allele (retrieved 2018-03-17)
[8]  https://en.wikipedia.org/wiki/Single-nucleotide_polymorphism (retrieved 2018-03-17)
[9] http://purl.obolibrary.org/obo/OGI_0000008 (retrieved 2018-03-17)
[10] http://purl.obolibrary.org/obo/OBI_0001352 (retrieved 2018-03-17)
[11] http://purl.phyloviz.net/ontology/typon#Allele (retrieved 2018-03-17)</ns3:IAO_0000116>
        <rdfs:comment>An allele is a seqeunce feature at a genomic location where variation occurs (i.e. where &gt;1 different sequence is known to exist). An allele can span only the extent of sequence known to vary (e.g. a single base SNP, or short insertion), or it can span a larger extent that includes one or more variable features as proper parts (e.g. a &#39;gene allele&#39; that spans the extent of an entire gene which contains several sequence alterations).

Alleles can carry &#39;reference&#39; or &#39;variant&#39; sequence - depending on whether the its &#39;state&#39; matches that considered to be the reference at that location. Alleles whose state differs from the reference are called &#39;variant alleles&#39;, and those that match the reference are called &#39;reference alleles&#39;. What is considered the &#39;reference&#39; state at a particular location may vary, depending on the context/goal of a particular analysis. A &#39;sequence alteration&#39; is a &#39;variant allele&#39; that varies along its entire extent (i.e every position varies from that of some defined reference sequence).</rdfs:comment>
        <ns3:IAO_0000115>One of a set of sequence features known to exist at a particular genomic location.</ns3:IAO_0000115>
        <ns3:IAO_0000118 xml:lang="en">variable feature</ns3:IAO_0000118>
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