Canonical Allele Identifier: CA1479946665

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318059A= , CM000666.2:g.99318059A=	GRCh38
NC_000004.11:g.100239216A= , CM000666.1:g.100239216A=	GRCh37
NC_000004.10:g.100458239A=	NCBI36
NG_011435.1:g.8357T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.246T= MANE Select	ENSP00000306606.8:p.Thr82=
ENST00000639454.1:c.246T=	ENSP00000491622.1:p.Thr82=
ENST00000305046.12:c.246T=	ENSP00000306606.8:p.Thr82=
ENST00000504498.1:n.300T=
ENST00000506651.5:c.126T=	ENSP00000425998.2:p.Thr42=
ENST00000515694.4:n.2341T=
ENST00000625860.2:c.126T=	ENSP00000486614.1:p.Thr42=
ENST00000632775.1:n.809T=
NM_000668.5:c.246T=	NP_000659.2:p.Thr82=
NM_001286650.1:c.126T=	NP_001273579.1:p.Thr42=
NM_000668.6:c.246T= MANE Select	NP_000659.2:p.Thr82=
NM_001286650.2:c.126T=	NP_001273579.1:p.Thr42=