Canonical Allele Identifier: CA2166452713
Gene: OCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28099007_28099008delinsAG , CM000677.2:g.28099007_28099008delinsAG GRCh38
NC_000015.9:g.28344153_28344154delinsAG , CM000677.1:g.28344153_28344154delinsAG GRCh37
NC_000015.8:g.26017748_26017749delinsAG NCBI36
NG_009846.1:g.5305_5306delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000354638.8:c.-22+216_-22+217delinsCT MANE Select ENSP00000346659.3:n.-22+216_-22+217delins...
ENST00000353809.9:c.-22+216_-22+217delinsCT ENSP00000261276.8:n.-22+216_-22+217delins...
ENST00000354638.7:c.-22+216_-22+217delinsCT ENSP00000346659.3:n.-22+216_-22+217delins...
ENST00000431101.1:c.-22+103_-22+104delinsCT ENSP00000415431.1:n.-22+103_-22+104delins...
ENST00000445578.5:c.-22+216_-22+217delinsCT ENSP00000414425.1:n.-22+216_-22+217delins...
NM_000275.2:c.-22+216_-22+217delinsCT NP_000266.2:n.-22+216_-22+217delinsCT
NM_001300984.1:c.-22+216_-22+217delinsCT NP_001287913.1:n.-22+216_-22+217delinsCT
XM_011521640.1:c.-22+216_-22+217delinsCT XP_011519942.1:n.-22+216_-22+217delinsCT
XM_011521640.2:c.-22+216_-22+217delinsCT XP_011519942.1:n.-22+216_-22+217delinsCT
NM_000275.3:c.-22+216_-22+217delinsCT MANE Select NP_000266.2:n.-22+216_-22+217delinsCT
NM_001300984.2:c.-22+216_-22+217delinsCT NP_001287913.1:n.-22+216_-22+217delinsCT