Canonical Allele Identifier: CA2166307671
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1595354025
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752097G>T , CM000677.2:g.27752097G>T GRCh38
NC_000015.9:g.27997243G>T , CM000677.1:g.27997243G>T GRCh37
NC_000015.8:g.25670838G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32769C>A XP_016877747.1:n.2457-32769C>A
XM_017022264.1:c.2292-32769C>A XP_016877753.1:n.2292-32769C>A
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