Canonical Allele Identifier: CA1479946651

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318028T= , CM000666.2:g.99318028T=	GRCh38
NC_000004.11:g.100239185T= , CM000666.1:g.100239185T=	GRCh37
NC_000004.10:g.100458208T=	NCBI36
NG_011435.1:g.8388A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.259+18A= MANE Select	ENSP00000306606.8:n.259+18A=
ENST00000639454.1:c.259+18A=	ENSP00000491622.1:n.259+18A=
ENST00000305046.12:c.259+18A=	ENSP00000306606.8:n.259+18A=
ENST00000504498.1:n.331A=
ENST00000506651.5:c.139+18A=	ENSP00000425998.2:n.139+18A=
ENST00000515694.4:n.2354+18A=
ENST00000625860.2:c.139+18A=	ENSP00000486614.1:n.139+18A=
ENST00000632775.1:n.840A=
NM_000668.5:c.259+18A=	NP_000659.2:n.259+18A=
NM_001286650.1:c.139+18A=	NP_001273579.1:n.139+18A=
NM_000668.6:c.259+18A= MANE Select	NP_000659.2:n.259+18A=
NM_001286650.2:c.139+18A=	NP_001273579.1:n.139+18A=