Canonical Allele Identifier: CA2762794020
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318240T>A , CM000666.2:g.99318240T>A GRCh38
NC_000004.11:g.100239397T>A , CM000666.1:g.100239397T>A GRCh37
NC_000004.10:g.100458420T>A NCBI36
NG_011435.1:g.8176A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.121-56A>T MANE Select ENSP00000306606.8:n.121-56A>T
ENST00000639454.1:c.121-56A>T ENSP00000491622.1:n.121-56A>T
ENST00000305046.12:c.121-56A>T ENSP00000306606.8:n.121-56A>T
ENST00000504498.1:n.175-56A>T
ENST00000506651.5:c.1-56A>T ENSP00000425998.2:n.1-56A>T
ENST00000515694.4:n.2216-56A>T
ENST00000625860.2:c.1-56A>T ENSP00000486614.1:n.1-56A>T
ENST00000632775.1:n.628A>T
NM_000668.5:c.121-56A>T NP_000659.2:n.121-56A>T
NM_001286650.1:c.1-56A>T NP_001273579.1:n.1-56A>T
NM_000668.6:c.121-56A>T MANE Select NP_000659.2:n.121-56A>T
NM_001286650.2:c.1-56A>T NP_001273579.1:n.1-56A>T