Canonical Allele Identifier: CA2515901644

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99317927C>T , CM000666.2:g.99317927C>T	GRCh38
NC_000004.11:g.100239084C>T , CM000666.1:g.100239084C>T	GRCh37
NC_000004.10:g.100458107C>T	NCBI36
NG_011435.1:g.8489G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.259+119G>A MANE Select	ENSP00000306606.8:n.259+119G>A
ENST00000639454.1:c.259+119G>A	ENSP00000491622.1:n.259+119G>A
ENST00000305046.12:c.259+119G>A	ENSP00000306606.8:n.259+119G>A
ENST00000504498.1:n.432G>A
ENST00000506651.5:c.139+119G>A	ENSP00000425998.2:n.139+119G>A
ENST00000515694.4:n.2354+119G>A
ENST00000625860.2:c.139+119G>A	ENSP00000486614.1:n.139+119G>A
ENST00000632775.1:n.941G>A
NM_000668.5:c.259+119G>A	NP_000659.2:n.259+119G>A
NM_001286650.1:c.139+119G>A	NP_001273579.1:n.139+119G>A
NM_000668.6:c.259+119G>A MANE Select	NP_000659.2:n.259+119G>A
NM_001286650.2:c.139+119G>A	NP_001273579.1:n.139+119G>A