Canonical Allele Identifier: CA1479946671

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318070C= , CM000666.2:g.99318070C=	GRCh38
NC_000004.11:g.100239227C= , CM000666.1:g.100239227C=	GRCh37
NC_000004.10:g.100458250C=	NCBI36
NG_011435.1:g.8346G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.235G= MANE Select	ENSP00000306606.8:p.Glu79=
ENST00000639454.1:c.235G=	ENSP00000491622.1:p.Glu79=
ENST00000305046.12:c.235G=	ENSP00000306606.8:p.Glu79=
ENST00000504498.1:n.289G=
ENST00000506651.5:c.115G=	ENSP00000425998.2:p.Glu39=
ENST00000515694.4:n.2330G=
ENST00000625860.2:c.115G=	ENSP00000486614.1:p.Glu39=
ENST00000632775.1:n.798G=
NM_000668.5:c.235G=	NP_000659.2:p.Glu79=
NM_001286650.1:c.115G=	NP_001273579.1:p.Glu39=
NM_000668.6:c.235G= MANE Select	NP_000659.2:p.Glu79=
NM_001286650.2:c.115G=	NP_001273579.1:p.Glu39=