Canonical Allele Identifier: CA268293506

Gene: OCA2

Linked Data

• dbSNP Id: rs563823393
• gnomAD v2: 15-27997211-T-C
• gnomAD v3: 15-27752065-T-C
• gnomAD v4: 15-27752065-T-C
• MyVariant Identifiers: chr15:g.27997211T>C (hg19) ; chr15:g.27752065T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27752065T>C , CM000677.2:g.27752065T>C	GRCh38
NC_000015.9:g.27997211T>C , CM000677.1:g.27997211T>C	GRCh37
NC_000015.8:g.25670806T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017022258.1:c.2457-32737A>G	XP_016877747.1:n.2457-32737A>G
XM_017022264.1:c.2292-32737A>G	XP_016877753.1:n.2292-32737A>G