Canonical Allele Identifier: CA357479058
Gene: ADH1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318066C>G , CM000666.2:g.99318066C>G GRCh38
NC_000004.11:g.100239223C>G , CM000666.1:g.100239223C>G GRCh37
NC_000004.10:g.100458246C>G NCBI36
NG_011435.1:g.8350G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.239G>C MANE Select ENSP00000306606.8:p.Gly80Ala
ENST00000639454.1:c.239G>C ENSP00000491622.1:p.Gly80Ala
ENST00000305046.12:c.239G>C ENSP00000306606.8:p.Gly80Ala
ENST00000504498.1:n.293G>C
ENST00000506651.5:c.119G>C ENSP00000425998.2:p.Gly40Ala
ENST00000515694.4:n.2334G>C
ENST00000625860.2:c.119G>C ENSP00000486614.1:p.Gly40Ala
ENST00000632775.1:n.802G>C
NM_000668.5:c.239G>C NP_000659.2:p.Gly80Ala
NM_001286650.1:c.119G>C NP_001273579.1:p.Gly40Ala
NM_000668.6:c.239G>C MANE Select NP_000659.2:p.Gly80Ala
NM_001286650.2:c.119G>C NP_001273579.1:p.Gly40Ala