Canonical Allele Identifier: CA488959329

Gene: OCA2

Linked Data

• MyVariant Identifiers: chr15:g.28171387A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926241A>T , CM000677.2:g.27926241A>T	GRCh38
NC_000015.9:g.28171387A>T , CM000677.1:g.28171387A>T	GRCh37
NC_000015.8:g.25844982A>T	NCBI36
NG_009846.1:g.178072T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.1965T>A MANE Select	ENSP00000346659.3:p.Ile655=
ENST00000353809.9:c.1893T>A	ENSP00000261276.8:p.Ile631=
ENST00000354638.7:c.1965T>A	ENSP00000346659.3:p.Ile655=
NM_000275.2:c.1965T>A	NP_000266.2:p.Ile655=
NM_001300984.1:c.1893T>A	NP_001287913.1:p.Ile631=
XM_011521639.1:c.1989T>A	XP_011519941.1:p.Ile663=
XM_011521640.1:c.1965T>A	XP_011519942.1:p.Ile655=
XM_011521641.1:c.1989T>A	XP_011519943.1:p.Ile663=
XM_011521642.1:c.1917T>A	XP_011519944.1:p.Ile639=
XM_011521643.1:c.1917T>A	XP_011519945.1:p.Ile639=
XM_011521644.1:c.1851T>A	XP_011519946.1:p.Ile617=
XM_011521645.1:c.1989T>A	XP_011519947.1:p.Ile663=
XM_011521640.2:c.1965T>A	XP_011519942.1:p.Ile655=
XM_017022255.1:c.1989T>A	XP_016877744.1:p.Ile663=
XM_017022256.1:c.1989T>A	XP_016877745.1:p.Ile663=
XM_017022257.1:c.1917T>A	XP_016877746.1:p.Ile639=
XM_017022258.1:c.1989T>A	XP_016877747.1:p.Ile663=
XM_017022259.1:c.1917T>A	XP_016877748.1:p.Ile639=
XM_017022260.1:c.1851T>A	XP_016877749.1:p.Ile617=
XM_017022261.1:c.1794T>A	XP_016877750.1:p.Ile598=
XM_017022262.1:c.1989T>A	XP_016877751.1:p.Ile663=
XM_017022263.1:c.1989T>A	XP_016877752.1:p.Ile663=
XM_017022264.1:c.1989T>A	XP_016877753.1:p.Ile663=
NM_000275.3:c.1965T>A MANE Select	NP_000266.2:p.Ile655=
NM_001300984.2:c.1893T>A	NP_001287913.1:p.Ile631=