Canonical Allele Identifier: CA391361323
Gene: OCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27926222G>T , CM000677.2:g.27926222G>T GRCh38
NC_000015.9:g.28171368G>T , CM000677.1:g.28171368G>T GRCh37
NC_000015.8:g.25844963G>T NCBI36
NG_009846.1:g.178091C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354638.8:c.1984C>A MANE Select ENSP00000346659.3:p.Leu662Ile
ENST00000353809.9:c.1912C>A ENSP00000261276.8:p.Leu638Ile
ENST00000354638.7:c.1984C>A ENSP00000346659.3:p.Leu662Ile
NM_000275.2:c.1984C>A NP_000266.2:p.Leu662Ile
NM_001300984.1:c.1912C>A NP_001287913.1:p.Leu638Ile
XM_011521639.1:c.2008C>A XP_011519941.1:p.Leu670Ile
XM_011521640.1:c.1984C>A XP_011519942.1:p.Leu662Ile
XM_011521641.1:c.2008C>A XP_011519943.1:p.Leu670Ile
XM_011521642.1:c.1936C>A XP_011519944.1:p.Leu646Ile
XM_011521643.1:c.1936C>A XP_011519945.1:p.Leu646Ile
XM_011521644.1:c.1870C>A XP_011519946.1:p.Leu624Ile
XM_011521645.1:c.2008C>A XP_011519947.1:p.Leu670Ile
XM_011521640.2:c.1984C>A XP_011519942.1:p.Leu662Ile
XM_017022255.1:c.2008C>A XP_016877744.1:p.Leu670Ile
XM_017022256.1:c.2008C>A XP_016877745.1:p.Leu670Ile
XM_017022257.1:c.1936C>A XP_016877746.1:p.Leu646Ile
XM_017022258.1:c.2008C>A XP_016877747.1:p.Leu670Ile
XM_017022259.1:c.1936C>A XP_016877748.1:p.Leu646Ile
XM_017022260.1:c.1870C>A XP_016877749.1:p.Leu624Ile
XM_017022261.1:c.1813C>A XP_016877750.1:p.Leu605Ile
XM_017022262.1:c.2008C>A XP_016877751.1:p.Leu670Ile
XM_017022263.1:c.2008C>A XP_016877752.1:p.Leu670Ile
XM_017022264.1:c.2008C>A XP_016877753.1:p.Leu670Ile
NM_000275.3:c.1984C>A MANE Select NP_000266.2:p.Leu662Ile
NM_001300984.2:c.1912C>A NP_001287913.1:p.Leu638Ile