Canonical Allele Identifier: CA1479946602

Gene: ADH1B

Linked Data

• dbSNP Id: rs1733925686
• gnomAD v4: 4-99317939-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99317939G>A , CM000666.2:g.99317939G>A	GRCh38
NC_000004.11:g.100239096G>A , CM000666.1:g.100239096G>A	GRCh37
NC_000004.10:g.100458119G>A	NCBI36
NG_011435.1:g.8477C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.259+107C>T MANE Select	ENSP00000306606.8:n.259+107C>T
ENST00000639454.1:c.259+107C>T	ENSP00000491622.1:n.259+107C>T
ENST00000305046.12:c.259+107C>T	ENSP00000306606.8:n.259+107C>T
ENST00000504498.1:n.420C>T
ENST00000506651.5:c.139+107C>T	ENSP00000425998.2:n.139+107C>T
ENST00000515694.4:n.2354+107C>T
ENST00000625860.2:c.139+107C>T	ENSP00000486614.1:n.139+107C>T
ENST00000632775.1:n.929C>T
NM_000668.5:c.259+107C>T	NP_000659.2:n.259+107C>T
NM_001286650.1:c.139+107C>T	NP_001273579.1:n.139+107C>T
NM_000668.6:c.259+107C>T MANE Select	NP_000659.2:n.259+107C>T
NM_001286650.2:c.139+107C>T	NP_001273579.1:n.139+107C>T