Canonical Allele Identifier: CA440300553

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239225T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318068T>C , CM000666.2:g.99318068T>C	GRCh38
NC_000004.11:g.100239225T>C , CM000666.1:g.100239225T>C	GRCh37
NC_000004.10:g.100458248T>C	NCBI36
NG_011435.1:g.8348A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.237A>G MANE Select	ENSP00000306606.8:p.Glu79=
ENST00000639454.1:c.237A>G	ENSP00000491622.1:p.Glu79=
ENST00000305046.12:c.237A>G	ENSP00000306606.8:p.Glu79=
ENST00000504498.1:n.291A>G
ENST00000506651.5:c.117A>G	ENSP00000425998.2:p.Glu39=
ENST00000515694.4:n.2332A>G
ENST00000625860.2:c.117A>G	ENSP00000486614.1:p.Glu39=
ENST00000632775.1:n.800A>G
NM_000668.5:c.237A>G	NP_000659.2:p.Glu79=
NM_001286650.1:c.117A>G	NP_001273579.1:p.Glu39=
NM_000668.6:c.237A>G MANE Select	NP_000659.2:p.Glu79=
NM_001286650.2:c.117A>G	NP_001273579.1:p.Glu39=