Canonical Allele Identifier: CA488959037

Gene: OCA2

Linked Data

• gnomAD v4: 15-27851404-C-G
• MyVariant Identifiers: chr15:g.28096550C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27851404C>G , CM000677.2:g.27851404C>G	GRCh38
NC_000015.9:g.28096550C>G , CM000677.1:g.28096550C>G	GRCh37
NC_000015.8:g.25770145C>G	NCBI36
NG_009846.1:g.252909G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.2316G>C MANE Select	ENSP00000346659.3:p.Leu772=
ENST00000353809.9:c.2244G>C	ENSP00000261276.8:p.Leu748=
ENST00000354638.7:c.2316G>C	ENSP00000346659.3:p.Leu772=
NM_000275.2:c.2316G>C	NP_000266.2:p.Leu772=
NM_001300984.1:c.2244G>C	NP_001287913.1:p.Leu748=
XM_011521639.1:c.2382G>C	XP_011519941.1:p.Leu794=
XM_011521640.1:c.2358G>C	XP_011519942.1:p.Leu786=
XM_011521641.1:c.2340G>C	XP_011519943.1:p.Leu780=
XM_011521642.1:c.2310G>C	XP_011519944.1:p.Leu770=
XM_011521643.1:c.2268G>C	XP_011519945.1:p.Leu756=
XM_011521644.1:c.2244G>C	XP_011519946.1:p.Leu748=
XM_011521645.1:c.2175G>C	XP_011519947.1:p.Leu725=
XM_011521640.2:c.2358G>C	XP_011519942.1:p.Leu786=
XM_017022255.1:c.2382G>C	XP_016877744.1:p.Leu794=
XM_017022256.1:c.2340G>C	XP_016877745.1:p.Leu780=
XM_017022257.1:c.2310G>C	XP_016877746.1:p.Leu770=
XM_017022258.1:c.2340G>C	XP_016877747.1:p.Leu780=
XM_017022259.1:c.2268G>C	XP_016877748.1:p.Leu756=
XM_017022260.1:c.2244G>C	XP_016877749.1:p.Leu748=
XM_017022261.1:c.2187G>C	XP_016877750.1:p.Leu729=
XM_017022262.1:c.2268+19750G>C	XP_016877751.1:n.2268+19750G>C
XM_017022263.1:c.2175G>C	XP_016877752.1:p.Leu725=
XM_017022264.1:c.2175G>C	XP_016877753.1:p.Leu725=
NM_000275.3:c.2316G>C MANE Select	NP_000266.2:p.Leu772=
NM_001300984.2:c.2244G>C	NP_001287913.1:p.Leu748=