Canonical Allele Identifier: CA1479942114
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307700T= , CM000666.2:g.99307700T= GRCh38
NC_000004.11:g.100228857T= , CM000666.1:g.100228857T= GRCh37
NC_000004.10:g.100447880T= NCBI36
NG_011435.1:g.18716A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*140A= MANE Select ENSP00000306606.8:n.*140A=
ENST00000305046.12:c.*140A= ENSP00000306606.8:n.*140A=
ENST00000506651.5:c.*140A= ENSP00000425998.2:n.*140A=
ENST00000515694.4:n.3363A=
ENST00000625860.2:c.*140A= ENSP00000486614.1:n.*140A=
NM_000668.5:c.*140A= NP_000659.2:n.*140A=
NM_001286650.1:c.*140A= NP_001273579.1:n.*140A=
NM_000668.6:c.*140A= MANE Select NP_000659.2:n.*140A=
NM_001286650.2:c.*140A= NP_001273579.1:n.*140A=