Canonical Allele Identifier: CA2166468689
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2044910529

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28093590T>C , CM000677.2:g.28093590T>C GRCh38
NC_000015.9:g.28338736T>C , CM000677.1:g.28338736T>C GRCh37
NC_000015.8:g.26012331T>C NCBI36
NG_009846.1:g.10723A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354638.8:c.-22+5634A>G MANE Select ENSP00000346659.3:n.-22+5634A>G
ENST00000353809.9:c.-22+5634A>G ENSP00000261276.8:n.-22+5634A>G
ENST00000354638.7:c.-22+5634A>G ENSP00000346659.3:n.-22+5634A>G
ENST00000431101.1:c.-22+5521A>G ENSP00000415431.1:n.-22+5521A>G
ENST00000445578.5:c.-22+5634A>G ENSP00000414425.1:n.-22+5634A>G
NM_000275.2:c.-22+5634A>G NP_000266.2:n.-22+5634A>G
NM_001300984.1:c.-22+5634A>G NP_001287913.1:n.-22+5634A>G
XM_011521640.1:c.-22+5634A>G XP_011519942.1:n.-22+5634A>G
XM_011521640.2:c.-22+5634A>G XP_011519942.1:n.-22+5634A>G
NM_000275.3:c.-22+5634A>G MANE Select NP_000266.2:n.-22+5634A>G
NM_001300984.2:c.-22+5634A>G NP_001287913.1:n.-22+5634A>G