Canonical Allele Identifier: CA1479942169

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307820G= , CM000666.2:g.99307820G=	GRCh38
NC_000004.11:g.100228977G= , CM000666.1:g.100228977G=	GRCh37
NC_000004.10:g.100448000G=	NCBI36
NG_011435.1:g.18596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*20C= MANE Select	ENSP00000306606.8:n.*20C=
ENST00000305046.12:c.*20C=	ENSP00000306606.8:n.*20C=
ENST00000506651.5:c.*20C=	ENSP00000425998.2:n.*20C=
ENST00000515694.4:n.3243C=
ENST00000625860.2:c.*20C=	ENSP00000486614.1:n.*20C=
NM_000668.5:c.*20C=	NP_000659.2:n.*20C=
NM_001286650.1:c.*20C=	NP_001273579.1:n.*20C=
NM_000668.6:c.*20C= MANE Select	NP_000659.2:n.*20C=
NM_001286650.2:c.*20C=	NP_001273579.1:n.*20C=