Canonical Allele Identifier: CA391361883
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1432167731

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28027917C>G , CM000677.2:g.28027917C>G GRCh38
NC_000015.9:g.28273063C>G , CM000677.1:g.28273063C>G GRCh37
NC_000015.8:g.25946658C>G NCBI36
NG_009846.1:g.76396G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354638.8:c.469G>C MANE Select ENSP00000346659.3:p.Asp157His
ENST00000353809.9:c.469G>C ENSP00000261276.8:p.Asp157His
ENST00000354638.7:c.469G>C ENSP00000346659.3:p.Asp157His
ENST00000431101.1:c.469G>C ENSP00000415431.1:p.Asp157His
ENST00000445578.5:c.469G>C ENSP00000414425.1:p.Asp157His
NM_000275.2:c.469G>C NP_000266.2:p.Asp157His
NM_001300984.1:c.469G>C NP_001287913.1:p.Asp157His
XM_011521639.1:c.493G>C XP_011519941.1:p.Asp165His
XM_011521640.1:c.469G>C XP_011519942.1:p.Asp157His
XM_011521641.1:c.493G>C XP_011519943.1:p.Asp165His
XM_011521642.1:c.493G>C XP_011519944.1:p.Asp165His
XM_011521643.1:c.493G>C XP_011519945.1:p.Asp165His
XM_011521644.1:c.493G>C XP_011519946.1:p.Asp165His
XM_011521645.1:c.493G>C XP_011519947.1:p.Asp165His
XM_011521646.1:c.493G>C XP_011519948.1:p.Asp165His
XM_011521647.1:c.493G>C XP_011519949.1:p.Asp165His
XR_931843.1:n.1854G>C
XM_011521640.2:c.469G>C XP_011519942.1:p.Asp157His
XM_017022255.1:c.493G>C XP_016877744.1:p.Asp165His
XM_017022256.1:c.493G>C XP_016877745.1:p.Asp165His
XM_017022257.1:c.493G>C XP_016877746.1:p.Asp165His
XM_017022258.1:c.493G>C XP_016877747.1:p.Asp165His
XM_017022259.1:c.493G>C XP_016877748.1:p.Asp165His
XM_017022260.1:c.493G>C XP_016877749.1:p.Asp165His
XM_017022261.1:c.298G>C XP_016877750.1:p.Asp100His
XM_017022262.1:c.493G>C XP_016877751.1:p.Asp165His
XM_017022263.1:c.493G>C XP_016877752.1:p.Asp165His
XM_017022264.1:c.493G>C XP_016877753.1:p.Asp165His
XM_017022265.1:c.493G>C XP_016877754.1:p.Asp165His
XR_001751294.1:n.582G>C
NM_000275.3:c.469G>C MANE Select NP_000266.2:p.Asp157His
NM_001300984.2:c.469G>C NP_001287913.1:p.Asp157His