Canonical Allele Identifier: CA1479942172

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307824A= , CM000666.2:g.99307824A=	GRCh38
NC_000004.11:g.100228981A= , CM000666.1:g.100228981A=	GRCh37
NC_000004.10:g.100448004A=	NCBI36
NG_011435.1:g.18592T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.*16T= MANE Select	ENSP00000306606.8:n.*16T=
ENST00000305046.12:c.*16T=	ENSP00000306606.8:n.*16T=
ENST00000506651.5:c.*16T=	ENSP00000425998.2:n.*16T=
ENST00000515694.4:n.3239T=
ENST00000625860.2:c.*16T=	ENSP00000486614.1:n.*16T=
NM_000668.5:c.*16T=	NP_000659.2:n.*16T=
NM_001286650.1:c.*16T=	NP_001273579.1:n.*16T=
NM_000668.6:c.*16T= MANE Select	NP_000659.2:n.*16T=
NM_001286650.2:c.*16T=	NP_001273579.1:n.*16T=