Canonical Allele Identifier: CA1479942159

Gene: ADH1B

Linked Data

• dbSNP Id: rs1733649170

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307808A>G , CM000666.2:g.99307808A>G	GRCh38
NC_000004.11:g.100228965A>G , CM000666.1:g.100228965A>G	GRCh37
NC_000004.10:g.100447988A>G	NCBI36
NG_011435.1:g.18608T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.*32T>C MANE Select	ENSP00000306606.8:n.*32T>C
ENST00000305046.12:c.*32T>C	ENSP00000306606.8:n.*32T>C
ENST00000506651.5:c.*32T>C	ENSP00000425998.2:n.*32T>C
ENST00000515694.4:n.3255T>C
ENST00000625860.2:c.*32T>C	ENSP00000486614.1:n.*32T>C
NM_000668.5:c.*32T>C	NP_000659.2:n.*32T>C
NM_001286650.1:c.*32T>C	NP_001273579.1:n.*32T>C
NM_000668.6:c.*32T>C MANE Select	NP_000659.2:n.*32T>C
NM_001286650.2:c.*32T>C	NP_001273579.1:n.*32T>C