Canonical Allele Identifier: CA1479946699

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318130C= , CM000666.2:g.99318130C=	GRCh38
NC_000004.11:g.100239287C= , CM000666.1:g.100239287C=	GRCh37
NC_000004.10:g.100458310C=	NCBI36
NG_011435.1:g.8286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.175G= MANE Select	ENSP00000306606.8:p.Val59=
ENST00000639454.1:c.175G=	ENSP00000491622.1:p.Val59=
ENST00000305046.12:c.175G=	ENSP00000306606.8:p.Val59=
ENST00000504498.1:n.229G=
ENST00000506651.5:c.55G=	ENSP00000425998.2:p.Val19=
ENST00000515694.4:n.2270G=
ENST00000625860.2:c.55G=	ENSP00000486614.1:p.Val19=
ENST00000632775.1:n.738G=
NM_000668.5:c.175G=	NP_000659.2:p.Val59=
NM_001286650.1:c.55G=	NP_001273579.1:p.Val19=
NM_000668.6:c.175G= MANE Select	NP_000659.2:p.Val59=
NM_001286650.2:c.55G=	NP_001273579.1:p.Val19=