Canonical Allele Identifier: CA711703743

Gene: OCA2

Linked Data

• dbSNP Id: rs1181677936
• gnomAD v3: 15-27752117-G-T
• gnomAD v4: 15-27752117-G-T
• MyVariant Identifiers: chr15:g.27997263G>T (hg19) ; chr15:g.27752117G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27752117G>T , CM000677.2:g.27752117G>T	GRCh38
NC_000015.9:g.27997263G>T , CM000677.1:g.27997263G>T	GRCh37
NC_000015.8:g.25670858G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_017022258.1:c.2457-32789C>A	XP_016877747.1:n.2457-32789C>A
XM_017022264.1:c.2292-32789C>A	XP_016877753.1:n.2292-32789C>A