Canonical Allele Identifier: CA440300592

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239261G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318104G>T , CM000666.2:g.99318104G>T	GRCh38
NC_000004.11:g.100239261G>T , CM000666.1:g.100239261G>T	GRCh37
NC_000004.10:g.100458284G>T	NCBI36
NG_011435.1:g.8312C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.201C>A MANE Select	ENSP00000306606.8:p.Gly67=
ENST00000639454.1:c.201C>A	ENSP00000491622.1:p.Gly67=
ENST00000305046.12:c.201C>A	ENSP00000306606.8:p.Gly67=
ENST00000504498.1:n.255C>A
ENST00000506651.5:c.81C>A	ENSP00000425998.2:p.Gly27=
ENST00000515694.4:n.2296C>A
ENST00000625860.2:c.81C>A	ENSP00000486614.1:p.Gly27=
ENST00000632775.1:n.764C>A
NM_000668.5:c.201C>A	NP_000659.2:p.Gly67=
NM_001286650.1:c.81C>A	NP_001273579.1:p.Gly27=
NM_000668.6:c.201C>A MANE Select	NP_000659.2:p.Gly67=
NM_001286650.2:c.81C>A	NP_001273579.1:p.Gly27=