Canonical Allele Identifier: CA391361409

Gene: OCA2

Linked Data

• dbSNP Id: rs1182502204
• gnomAD v3: 15-27926245-G-A
• gnomAD v4: 15-27926245-G-A
• MyVariant Identifiers: chr15:g.28171391G>A (hg19) ; chr15:g.27926245G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926245G>A , CM000677.2:g.27926245G>A	GRCh38
NC_000015.9:g.28171391G>A , CM000677.1:g.28171391G>A	GRCh37
NC_000015.8:g.25844986G>A	NCBI36
NG_009846.1:g.178068C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.1961C>T MANE Select	ENSP00000346659.3:p.Ala654Val
ENST00000353809.9:c.1889C>T	ENSP00000261276.8:p.Ala630Val
ENST00000354638.7:c.1961C>T	ENSP00000346659.3:p.Ala654Val
NM_000275.2:c.1961C>T	NP_000266.2:p.Ala654Val
NM_001300984.1:c.1889C>T	NP_001287913.1:p.Ala630Val
XM_011521639.1:c.1985C>T	XP_011519941.1:p.Ala662Val
XM_011521640.1:c.1961C>T	XP_011519942.1:p.Ala654Val
XM_011521641.1:c.1985C>T	XP_011519943.1:p.Ala662Val
XM_011521642.1:c.1913C>T	XP_011519944.1:p.Ala638Val
XM_011521643.1:c.1913C>T	XP_011519945.1:p.Ala638Val
XM_011521644.1:c.1847C>T	XP_011519946.1:p.Ala616Val
XM_011521645.1:c.1985C>T	XP_011519947.1:p.Ala662Val
XM_011521640.2:c.1961C>T	XP_011519942.1:p.Ala654Val
XM_017022255.1:c.1985C>T	XP_016877744.1:p.Ala662Val
XM_017022256.1:c.1985C>T	XP_016877745.1:p.Ala662Val
XM_017022257.1:c.1913C>T	XP_016877746.1:p.Ala638Val
XM_017022258.1:c.1985C>T	XP_016877747.1:p.Ala662Val
XM_017022259.1:c.1913C>T	XP_016877748.1:p.Ala638Val
XM_017022260.1:c.1847C>T	XP_016877749.1:p.Ala616Val
XM_017022261.1:c.1790C>T	XP_016877750.1:p.Ala597Val
XM_017022262.1:c.1985C>T	XP_016877751.1:p.Ala662Val
XM_017022263.1:c.1985C>T	XP_016877752.1:p.Ala662Val
XM_017022264.1:c.1985C>T	XP_016877753.1:p.Ala662Val
NM_000275.3:c.1961C>T MANE Select	NP_000266.2:p.Ala654Val
NM_001300984.2:c.1889C>T	NP_001287913.1:p.Ala630Val