Canonical Allele Identifier: CA1479946587

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99317905G= , CM000666.2:g.99317905G=	GRCh38
NC_000004.11:g.100239062G= , CM000666.1:g.100239062G=	GRCh37
NC_000004.10:g.100458085G=	NCBI36
NG_011435.1:g.8511C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.259+141C= MANE Select	ENSP00000306606.8:n.259+141C=
ENST00000639454.1:c.259+141C=	ENSP00000491622.1:n.259+141C=
ENST00000305046.12:c.259+141C=	ENSP00000306606.8:n.259+141C=
ENST00000504498.1:n.454C=
ENST00000506651.5:c.139+141C=	ENSP00000425998.2:n.139+141C=
ENST00000515694.4:n.2354+141C=
ENST00000625860.2:c.139+141C=	ENSP00000486614.1:n.139+141C=
ENST00000632775.1:n.963C=
NM_000668.5:c.259+141C=	NP_000659.2:n.259+141C=
NM_001286650.1:c.139+141C=	NP_001273579.1:n.139+141C=
NM_000668.6:c.259+141C= MANE Select	NP_000659.2:n.259+141C=
NM_001286650.2:c.139+141C=	NP_001273579.1:n.139+141C=