Canonical Allele Identifier: CA357479071
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100239225T>G (hg19) chr4:g.99318068T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318068T>G , CM000666.2:g.99318068T>G GRCh38
NC_000004.11:g.100239225T>G , CM000666.1:g.100239225T>G GRCh37
NC_000004.10:g.100458248T>G NCBI36
NG_011435.1:g.8348A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.237A>C MANE Select ENSP00000306606.8:p.Glu79Asp
ENST00000639454.1:c.237A>C ENSP00000491622.1:p.Glu79Asp
ENST00000305046.12:c.237A>C ENSP00000306606.8:p.Glu79Asp
ENST00000504498.1:n.291A>C
ENST00000506651.5:c.117A>C ENSP00000425998.2:p.Glu39Asp
ENST00000515694.4:n.2332A>C
ENST00000625860.2:c.117A>C ENSP00000486614.1:p.Glu39Asp
ENST00000632775.1:n.800A>C
NM_000668.5:c.237A>C NP_000659.2:p.Glu79Asp
NM_001286650.1:c.117A>C NP_001273579.1:p.Glu39Asp
NM_000668.6:c.237A>C MANE Select NP_000659.2:p.Glu79Asp
NM_001286650.2:c.117A>C NP_001273579.1:p.Glu39Asp
Search 100 bp 5'
Search 100 bp 3'