Canonical Allele Identifier: CA488959010

Gene: OCA2

Linked Data

• MyVariant Identifiers: chr15:g.28096529T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27851383T>G , CM000677.2:g.27851383T>G	GRCh38
NC_000015.9:g.28096529T>G , CM000677.1:g.28096529T>G	GRCh37
NC_000015.8:g.25770124T>G	NCBI36
NG_009846.1:g.252930A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.2337A>C MANE Select	ENSP00000346659.3:p.Gly779=
ENST00000353809.9:c.2265A>C	ENSP00000261276.8:p.Gly755=
ENST00000354638.7:c.2337A>C	ENSP00000346659.3:p.Gly779=
NM_000275.2:c.2337A>C	NP_000266.2:p.Gly779=
NM_001300984.1:c.2265A>C	NP_001287913.1:p.Gly755=
XM_011521639.1:c.2403A>C	XP_011519941.1:p.Gly801=
XM_011521640.1:c.2379A>C	XP_011519942.1:p.Gly793=
XM_011521641.1:c.2361A>C	XP_011519943.1:p.Gly787=
XM_011521642.1:c.2331A>C	XP_011519944.1:p.Gly777=
XM_011521643.1:c.2289A>C	XP_011519945.1:p.Gly763=
XM_011521644.1:c.2265A>C	XP_011519946.1:p.Gly755=
XM_011521645.1:c.2196A>C	XP_011519947.1:p.Gly732=
XM_011521640.2:c.2379A>C	XP_011519942.1:p.Gly793=
XM_017022255.1:c.2403A>C	XP_016877744.1:p.Gly801=
XM_017022256.1:c.2361A>C	XP_016877745.1:p.Gly787=
XM_017022257.1:c.2331A>C	XP_016877746.1:p.Gly777=
XM_017022258.1:c.2361A>C	XP_016877747.1:p.Gly787=
XM_017022259.1:c.2289A>C	XP_016877748.1:p.Gly763=
XM_017022260.1:c.2265A>C	XP_016877749.1:p.Gly755=
XM_017022261.1:c.2208A>C	XP_016877750.1:p.Gly736=
XM_017022262.1:c.2268+19771A>C	XP_016877751.1:n.2268+19771A>C
XM_017022263.1:c.2196A>C	XP_016877752.1:p.Gly732=
XM_017022264.1:c.2196A>C	XP_016877753.1:p.Gly732=
NM_000275.3:c.2337A>C MANE Select	NP_000266.2:p.Gly779=
NM_001300984.2:c.2265A>C	NP_001287913.1:p.Gly755=