Canonical Allele Identifier: CA711703765

Gene: OCA2

Linked Data

• dbSNP Id: rs1317231744
• gnomAD v3: 15-27752178-C-A
• gnomAD v4: 15-27752178-C-A
• MyVariant Identifiers: chr15:g.27997324C>A (hg19) ; chr15:g.27752178C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27752178C>A , CM000677.2:g.27752178C>A	GRCh38
NC_000015.9:g.27997324C>A , CM000677.1:g.27997324C>A	GRCh37
NC_000015.8:g.25670919C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017022258.1:c.2457-32850G>T	XP_016877747.1:n.2457-32850G>T
XM_017022264.1:c.2292-32850G>T	XP_016877753.1:n.2292-32850G>T