Canonical Allele Identifier: CA488959105

Gene: OCA2

Linked Data

• MyVariant Identifiers: chr15:g.28096604G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27851458G>A , CM000677.2:g.27851458G>A	GRCh38
NC_000015.9:g.28096604G>A , CM000677.1:g.28096604G>A	GRCh37
NC_000015.8:g.25770199G>A	NCBI36
NG_009846.1:g.252855C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.2262C>T MANE Select	ENSP00000346659.3:p.Asn754=
ENST00000353809.9:c.2190C>T	ENSP00000261276.8:p.Asn730=
ENST00000354638.7:c.2262C>T	ENSP00000346659.3:p.Asn754=
NM_000275.2:c.2262C>T	NP_000266.2:p.Asn754=
NM_001300984.1:c.2190C>T	NP_001287913.1:p.Asn730=
XM_011521639.1:c.2328C>T	XP_011519941.1:p.Asn776=
XM_011521640.1:c.2304C>T	XP_011519942.1:p.Asn768=
XM_011521641.1:c.2286C>T	XP_011519943.1:p.Asn762=
XM_011521642.1:c.2256C>T	XP_011519944.1:p.Asn752=
XM_011521643.1:c.2214C>T	XP_011519945.1:p.Asn738=
XM_011521644.1:c.2190C>T	XP_011519946.1:p.Asn730=
XM_011521645.1:c.2121C>T	XP_011519947.1:p.Asn707=
XM_011521640.2:c.2304C>T	XP_011519942.1:p.Asn768=
XM_017022255.1:c.2328C>T	XP_016877744.1:p.Asn776=
XM_017022256.1:c.2286C>T	XP_016877745.1:p.Asn762=
XM_017022257.1:c.2256C>T	XP_016877746.1:p.Asn752=
XM_017022258.1:c.2286C>T	XP_016877747.1:p.Asn762=
XM_017022259.1:c.2214C>T	XP_016877748.1:p.Asn738=
XM_017022260.1:c.2190C>T	XP_016877749.1:p.Asn730=
XM_017022261.1:c.2133C>T	XP_016877750.1:p.Asn711=
XM_017022262.1:c.2268+19696C>T	XP_016877751.1:n.2268+19696C>T
XM_017022263.1:c.2121C>T	XP_016877752.1:p.Asn707=
XM_017022264.1:c.2121C>T	XP_016877753.1:p.Asn707=
NM_000275.3:c.2262C>T MANE Select	NP_000266.2:p.Asn754=
NM_001300984.2:c.2190C>T	NP_001287913.1:p.Asn730=