Canonical Allele Identifier: CA711703722

Gene: OCA2

Linked Data

• dbSNP Id: rs1470012592
• gnomAD v3: 15-27752083-C-T
• gnomAD v4: 15-27752083-C-T
• MyVariant Identifiers: chr15:g.27997229C>T (hg19) ; chr15:g.27752083C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27752083C>T , CM000677.2:g.27752083C>T	GRCh38
NC_000015.9:g.27997229C>T , CM000677.1:g.27997229C>T	GRCh37
NC_000015.8:g.25670824C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017022258.1:c.2457-32755G>A	XP_016877747.1:n.2457-32755G>A
XM_017022264.1:c.2292-32755G>A	XP_016877753.1:n.2292-32755G>A