Canonical Allele Identifier: CA1479942165
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307817C= , CM000666.2:g.99307817C= GRCh38
NC_000004.11:g.100228974C= , CM000666.1:g.100228974C= GRCh37
NC_000004.10:g.100447997C= NCBI36
NG_011435.1:g.18599G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*23G= MANE Select ENSP00000306606.8:n.*23G=
ENST00000305046.12:c.*23G= ENSP00000306606.8:n.*23G=
ENST00000506651.5:c.*23G= ENSP00000425998.2:n.*23G=
ENST00000515694.4:n.3246G=
ENST00000625860.2:c.*23G= ENSP00000486614.1:n.*23G=
NM_000668.5:c.*23G= NP_000659.2:n.*23G=
NM_001286650.1:c.*23G= NP_001273579.1:n.*23G=
NM_000668.6:c.*23G= MANE Select NP_000659.2:n.*23G=
NM_001286650.2:c.*23G= NP_001273579.1:n.*23G=