Canonical Allele Identifier: CA357479500

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100239310T>A (hg19) ; chr4:g.99318153T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.152A>T MANE Select	ENSP00000306606.8:p.Asp51Val
ENST00000639454.1:c.152A>T	ENSP00000491622.1:p.Asp51Val
ENST00000305046.12:c.152A>T	ENSP00000306606.8:p.Asp51Val
ENST00000504498.1:n.206A>T
ENST00000506651.5:c.32A>T	ENSP00000425998.2:p.Asp11Val
ENST00000515694.4:n.2247A>T
ENST00000625860.2:c.32A>T	ENSP00000486614.1:p.Asp11Val
ENST00000632775.1:n.715A>T
NM_000668.5:c.152A>T	NP_000659.2:p.Asp51Val
NM_001286650.1:c.32A>T	NP_001273579.1:p.Asp11Val
NM_000668.6:c.152A>T MANE Select	NP_000659.2:p.Asp51Val
NM_001286650.2:c.32A>T	NP_001273579.1:p.Asp11Val