Canonical Allele Identifier: CA357479498

Gene: ADH1B

Linked Data

• gnomAD v4: 4-99318153-T-C
• MyVariant Identifiers: chr4:g.100239310T>C (hg19) ; chr4:g.99318153T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99318153T>C , CM000666.2:g.99318153T>C	GRCh38
NC_000004.11:g.100239310T>C , CM000666.1:g.100239310T>C	GRCh37
NC_000004.10:g.100458333T>C	NCBI36
NG_011435.1:g.8263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.152A>G MANE Select	ENSP00000306606.8:p.Asp51Gly
ENST00000639454.1:c.152A>G	ENSP00000491622.1:p.Asp51Gly
ENST00000305046.12:c.152A>G	ENSP00000306606.8:p.Asp51Gly
ENST00000504498.1:n.206A>G
ENST00000506651.5:c.32A>G	ENSP00000425998.2:p.Asp11Gly
ENST00000515694.4:n.2247A>G
ENST00000625860.2:c.32A>G	ENSP00000486614.1:p.Asp11Gly
ENST00000632775.1:n.715A>G
NM_000668.5:c.152A>G	NP_000659.2:p.Asp51Gly
NM_001286650.1:c.32A>G	NP_001273579.1:p.Asp11Gly
NM_000668.6:c.152A>G MANE Select	NP_000659.2:p.Asp51Gly
NM_001286650.2:c.32A>G	NP_001273579.1:p.Asp11Gly