Canonical Allele Identifier: CA2166409914

Gene: OCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27983350T= , CM000677.2:g.27983350T=	GRCh38
NC_000015.9:g.28228496T= , CM000677.1:g.28228496T=	GRCh37
NC_000015.8:g.25902091T=	NCBI36
NG_009846.1:g.120963A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.1498A= MANE Select	ENSP00000346659.3:p.Lys500=
ENST00000353809.9:c.1426A=	ENSP00000261276.8:p.Lys476=
ENST00000354638.7:c.1498A=	ENSP00000346659.3:p.Lys500=
NM_000275.2:c.1498A=	NP_000266.2:p.Lys500=
NM_001300984.1:c.1426A=	NP_001287913.1:p.Lys476=
XM_011521639.1:c.1522A=	XP_011519941.1:p.Lys508=
XM_011521640.1:c.1498A=	XP_011519942.1:p.Lys500=
XM_011521641.1:c.1522A=	XP_011519943.1:p.Lys508=
XM_011521642.1:c.1450A=	XP_011519944.1:p.Lys484=
XM_011521643.1:c.1450A=	XP_011519945.1:p.Lys484=
XM_011521644.1:c.1384A=	XP_011519946.1:p.Lys462=
XM_011521645.1:c.1522A=	XP_011519947.1:p.Lys508=
XM_011521646.1:c.1522A=	XP_011519948.1:p.Lys508=
XM_011521647.1:c.1522A=	XP_011519949.1:p.Lys508=
XR_931843.1:n.2883A=
XM_011521640.2:c.1498A=	XP_011519942.1:p.Lys500=
XM_017022255.1:c.1522A=	XP_016877744.1:p.Lys508=
XM_017022256.1:c.1522A=	XP_016877745.1:p.Lys508=
XM_017022257.1:c.1450A=	XP_016877746.1:p.Lys484=
XM_017022258.1:c.1522A=	XP_016877747.1:p.Lys508=
XM_017022259.1:c.1450A=	XP_016877748.1:p.Lys484=
XM_017022260.1:c.1384A=	XP_016877749.1:p.Lys462=
XM_017022261.1:c.1327A=	XP_016877750.1:p.Lys443=
XM_017022262.1:c.1522A=	XP_016877751.1:p.Lys508=
XM_017022263.1:c.1522A=	XP_016877752.1:p.Lys508=
XM_017022264.1:c.1522A=	XP_016877753.1:p.Lys508=
XM_017022265.1:c.1522A=	XP_016877754.1:p.Lys508=
XR_001751294.1:n.1611A=
NM_000275.3:c.1498A= MANE Select	NP_000266.2:p.Lys500=
NM_001300984.2:c.1426A=	NP_001287913.1:p.Lys476=