Canonical Allele Identifier: CA391361425

Gene: OCA2

Linked Data

• dbSNP Id: rs778788354
• gnomAD v3: 15-27926246-C-G
• gnomAD v4: 15-27926246-C-G
• MyVariant Identifiers: chr15:g.28171392C>G (hg19) ; chr15:g.27926246C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926246C>G , CM000677.2:g.27926246C>G	GRCh38
NC_000015.9:g.28171392C>G , CM000677.1:g.28171392C>G	GRCh37
NC_000015.8:g.25844987C>G	NCBI36
NG_009846.1:g.178067G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.1960G>C MANE Select	ENSP00000346659.3:p.Ala654Pro
ENST00000353809.9:c.1888G>C	ENSP00000261276.8:p.Ala630Pro
ENST00000354638.7:c.1960G>C	ENSP00000346659.3:p.Ala654Pro
NM_000275.2:c.1960G>C	NP_000266.2:p.Ala654Pro
NM_001300984.1:c.1888G>C	NP_001287913.1:p.Ala630Pro
XM_011521639.1:c.1984G>C	XP_011519941.1:p.Ala662Pro
XM_011521640.1:c.1960G>C	XP_011519942.1:p.Ala654Pro
XM_011521641.1:c.1984G>C	XP_011519943.1:p.Ala662Pro
XM_011521642.1:c.1912G>C	XP_011519944.1:p.Ala638Pro
XM_011521643.1:c.1912G>C	XP_011519945.1:p.Ala638Pro
XM_011521644.1:c.1846G>C	XP_011519946.1:p.Ala616Pro
XM_011521645.1:c.1984G>C	XP_011519947.1:p.Ala662Pro
XM_011521640.2:c.1960G>C	XP_011519942.1:p.Ala654Pro
XM_017022255.1:c.1984G>C	XP_016877744.1:p.Ala662Pro
XM_017022256.1:c.1984G>C	XP_016877745.1:p.Ala662Pro
XM_017022257.1:c.1912G>C	XP_016877746.1:p.Ala638Pro
XM_017022258.1:c.1984G>C	XP_016877747.1:p.Ala662Pro
XM_017022259.1:c.1912G>C	XP_016877748.1:p.Ala638Pro
XM_017022260.1:c.1846G>C	XP_016877749.1:p.Ala616Pro
XM_017022261.1:c.1789G>C	XP_016877750.1:p.Ala597Pro
XM_017022262.1:c.1984G>C	XP_016877751.1:p.Ala662Pro
XM_017022263.1:c.1984G>C	XP_016877752.1:p.Ala662Pro
XM_017022264.1:c.1984G>C	XP_016877753.1:p.Ala662Pro
NM_000275.3:c.1960G>C MANE Select	NP_000266.2:p.Ala654Pro
NM_001300984.2:c.1888G>C	NP_001287913.1:p.Ala630Pro