Canonical Allele Identifier: CA7438661

Gene: OCA2

Linked Data

• ClinVar Variation Id: 1413857
• ClinVar RCV Id: RCV001928359
• dbSNP Id: rs752888326
• ExAC: 15:28096593 T / A
• gnomAD v2: 15-28096593-T-A
• gnomAD v3: 15-27851447-T-A
• gnomAD v4: 15-27851447-T-A
• MyVariant Identifiers: chr15:g.28096593T>A (hg19) ; chr15:g.27851447T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27851447T>A , CM000677.2:g.27851447T>A	GRCh38
NC_000015.9:g.28096593T>A , CM000677.1:g.28096593T>A	GRCh37
NC_000015.8:g.25770188T>A	NCBI36
NG_009846.1:g.252866A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.2273A>T MANE Select	ENSP00000346659.3:p.Asp758Val
ENST00000353809.9:c.2201A>T	ENSP00000261276.8:p.Asp734Val
ENST00000354638.7:c.2273A>T	ENSP00000346659.3:p.Asp758Val
NM_000275.2:c.2273A>T	NP_000266.2:p.Asp758Val
NM_001300984.1:c.2201A>T	NP_001287913.1:p.Asp734Val
XM_011521639.1:c.2339A>T	XP_011519941.1:p.Asp780Val
XM_011521640.1:c.2315A>T	XP_011519942.1:p.Asp772Val
XM_011521641.1:c.2297A>T	XP_011519943.1:p.Asp766Val
XM_011521642.1:c.2267A>T	XP_011519944.1:p.Asp756Val
XM_011521643.1:c.2225A>T	XP_011519945.1:p.Asp742Val
XM_011521644.1:c.2201A>T	XP_011519946.1:p.Asp734Val
XM_011521645.1:c.2132A>T	XP_011519947.1:p.Asp711Val
XM_011521640.2:c.2315A>T	XP_011519942.1:p.Asp772Val
XM_017022255.1:c.2339A>T	XP_016877744.1:p.Asp780Val
XM_017022256.1:c.2297A>T	XP_016877745.1:p.Asp766Val
XM_017022257.1:c.2267A>T	XP_016877746.1:p.Asp756Val
XM_017022258.1:c.2297A>T	XP_016877747.1:p.Asp766Val
XM_017022259.1:c.2225A>T	XP_016877748.1:p.Asp742Val
XM_017022260.1:c.2201A>T	XP_016877749.1:p.Asp734Val
XM_017022261.1:c.2144A>T	XP_016877750.1:p.Asp715Val
XM_017022262.1:c.2268+19707A>T	XP_016877751.1:n.2268+19707A>T
XM_017022263.1:c.2132A>T	XP_016877752.1:p.Asp711Val
XM_017022264.1:c.2132A>T	XP_016877753.1:p.Asp711Val
NM_000275.3:c.2273A>T MANE Select	NP_000266.2:p.Asp758Val
NM_001300984.2:c.2201A>T	NP_001287913.1:p.Asp734Val