Canonical Allele Identifier: CA268293511
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs17565841

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752101G>A , CM000677.2:g.27752101G>A GRCh38
NC_000015.9:g.27997247G>A , CM000677.1:g.27997247G>A GRCh37
NC_000015.8:g.25670842G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32773C>T XP_016877747.1:p.=
XM_017022264.1:c.2292-32773C>T XP_016877753.1:p.=