Canonical Allele Identifier: CA2166307663
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1566934887
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752084G>A , CM000677.2:g.27752084G>A GRCh38
NC_000015.9:g.27997230G>A , CM000677.1:g.27997230G>A GRCh37
NC_000015.8:g.25670825G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017022258.1:c.2457-32756C>T XP_016877747.1:n.2457-32756C>T
XM_017022264.1:c.2292-32756C>T XP_016877753.1:n.2292-32756C>T
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