Canonical Allele Identifier: CA1479943768

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99311443T= , CM000666.2:g.99311443T=	GRCh38
NC_000004.11:g.100232600T= , CM000666.1:g.100232600T=	GRCh37
NC_000004.10:g.100451623T=	NCBI36
NG_011435.1:g.14973A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.964+78A= MANE Select	ENSP00000306606.8:n.964+78A=
ENST00000639454.1:c.964+78A=	ENSP00000491622.1:n.964+78A=
ENST00000305046.12:c.964+78A=	ENSP00000306606.8:n.964+78A=
ENST00000506651.5:c.844+78A=	ENSP00000425998.2:n.844+78A=
ENST00000515694.4:n.3059+78A=
ENST00000625860.2:c.844+78A=	ENSP00000486614.1:n.844+78A=
NM_000668.5:c.964+78A=	NP_000659.2:n.964+78A=
NM_001286650.1:c.844+78A=	NP_001273579.1:n.844+78A=
NM_000668.6:c.964+78A= MANE Select	NP_000659.2:n.964+78A=
NM_001286650.2:c.844+78A=	NP_001273579.1:n.844+78A=