Canonical Allele Identifier: CA440312023

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100228998C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307841C>T , CM000666.2:g.99307841C>T	GRCh38
NC_000004.11:g.100228998C>T , CM000666.1:g.100228998C>T	GRCh37
NC_000004.10:g.100448021C>T	NCBI36
NG_011435.1:g.18575G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.1127G>A MANE Select	ENSP00000306606.8:p.Ter376=
ENST00000305046.12:c.1127G>A	ENSP00000306606.8:p.Ter376=
ENST00000506651.5:c.1007G>A	ENSP00000425998.2:p.Ter336=
ENST00000515694.4:n.3222G>A
ENST00000625860.2:c.1007G>A	ENSP00000486614.1:p.Ter336=
NM_000668.5:c.1127G>A	NP_000659.2:p.Ter376=
NM_001286650.1:c.1007G>A	NP_001273579.1:p.Ter336=
NM_000668.6:c.1127G>A MANE Select	NP_000659.2:p.Ter376=
NM_001286650.2:c.1007G>A	NP_001273579.1:p.Ter336=