Canonical Allele Identifier: CA1479946685
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318092G= , CM000666.2:g.99318092G= GRCh38
NC_000004.11:g.100239249G= , CM000666.1:g.100239249G= GRCh37
NC_000004.10:g.100458272G= NCBI36
NG_011435.1:g.8324C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.213C= MANE Select ENSP00000306606.8:p.Ala71=
ENST00000639454.1:c.213C= ENSP00000491622.1:p.Ala71=
ENST00000305046.12:c.213C= ENSP00000306606.8:p.Ala71=
ENST00000504498.1:n.267C=
ENST00000506651.5:c.93C= ENSP00000425998.2:p.Ala31=
ENST00000515694.4:n.2308C=
ENST00000625860.2:c.93C= ENSP00000486614.1:p.Ala31=
ENST00000632775.1:n.776C=
NM_000668.5:c.213C= NP_000659.2:p.Ala71=
NM_001286650.1:c.93C= NP_001273579.1:p.Ala31=
NM_000668.6:c.213C= MANE Select NP_000659.2:p.Ala71=
NM_001286650.2:c.93C= NP_001273579.1:p.Ala31=