Canonical Allele Identifier: CA800703856

Gene: ADH1B

Linked Data

• dbSNP Id: rs1485316051
• gnomAD v4: 4-99317920-C-T
• MyVariant Identifiers: chr4:g.100239077C>T (hg19) ; chr4:g.99317920C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99317920C>T , CM000666.2:g.99317920C>T	GRCh38
NC_000004.11:g.100239077C>T , CM000666.1:g.100239077C>T	GRCh37
NC_000004.10:g.100458100C>T	NCBI36
NG_011435.1:g.8496G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000305046.13:c.259+126G>A MANE Select	ENSP00000306606.8:n.259+126G>A
ENST00000639454.1:c.259+126G>A	ENSP00000491622.1:n.259+126G>A
ENST00000305046.12:c.259+126G>A	ENSP00000306606.8:n.259+126G>A
ENST00000504498.1:n.439G>A
ENST00000506651.5:c.139+126G>A	ENSP00000425998.2:n.139+126G>A
ENST00000515694.4:n.2354+126G>A
ENST00000625860.2:c.139+126G>A	ENSP00000486614.1:n.139+126G>A
ENST00000632775.1:n.948G>A
NM_000668.5:c.259+126G>A	NP_000659.2:n.259+126G>A
NM_001286650.1:c.139+126G>A	NP_001273579.1:n.139+126G>A
NM_000668.6:c.259+126G>A MANE Select	NP_000659.2:n.259+126G>A
NM_001286650.2:c.139+126G>A	NP_001273579.1:n.139+126G>A