Canonical Allele Identifier: CA440300557

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239228T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318071T>G , CM000666.2:g.99318071T>G	GRCh38
NC_000004.11:g.100239228T>G , CM000666.1:g.100239228T>G	GRCh37
NC_000004.10:g.100458251T>G	NCBI36
NG_011435.1:g.8345A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.234A>C MANE Select	ENSP00000306606.8:p.Gly78=
ENST00000639454.1:c.234A>C	ENSP00000491622.1:p.Gly78=
ENST00000305046.12:c.234A>C	ENSP00000306606.8:p.Gly78=
ENST00000504498.1:n.288A>C
ENST00000506651.5:c.114A>C	ENSP00000425998.2:p.Gly38=
ENST00000515694.4:n.2329A>C
ENST00000625860.2:c.114A>C	ENSP00000486614.1:p.Gly38=
ENST00000632775.1:n.797A>C
NM_000668.5:c.234A>C	NP_000659.2:p.Gly78=
NM_001286650.1:c.114A>C	NP_001273579.1:p.Gly38=
NM_000668.6:c.234A>C MANE Select	NP_000659.2:p.Gly78=
NM_001286650.2:c.114A>C	NP_001273579.1:p.Gly38=