Canonical Allele Identifier: CA1479946718
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318171C= , CM000666.2:g.99318171C= GRCh38
NC_000004.11:g.100239328C= , CM000666.1:g.100239328C= GRCh37
NC_000004.10:g.100458351C= NCBI36
NG_011435.1:g.8245G=

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.134G= MANE Select ENSP00000306606.8:p.Gly45=
ENST00000639454.1:c.134G= ENSP00000491622.1:p.Gly45=
ENST00000305046.12:c.134G= ENSP00000306606.8:p.Gly45=
ENST00000504498.1:n.188G=
ENST00000506651.5:c.14G= ENSP00000425998.2:p.Gly5=
ENST00000515694.4:n.2229G=
ENST00000625860.2:c.14G= ENSP00000486614.1:p.Gly5=
ENST00000632775.1:n.697G=
NM_000668.5:c.134G= NP_000659.2:p.Gly45=
NM_001286650.1:c.14G= NP_001273579.1:p.Gly5=
NM_000668.6:c.134G= MANE Select NP_000659.2:p.Gly45=
NM_001286650.2:c.14G= NP_001273579.1:p.Gly5=