Canonical Allele Identifier: CA440300562
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100239231A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318074A>T , CM000666.2:g.99318074A>T GRCh38
NC_000004.11:g.100239231A>T , CM000666.1:g.100239231A>T GRCh37
NC_000004.10:g.100458254A>T NCBI36
NG_011435.1:g.8342T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.231T>A MANE Select ENSP00000306606.8:p.Val77=
ENST00000639454.1:c.231T>A ENSP00000491622.1:p.Val77=
ENST00000305046.12:c.231T>A ENSP00000306606.8:p.Val77=
ENST00000504498.1:n.285T>A
ENST00000506651.5:c.111T>A ENSP00000425998.2:p.Val37=
ENST00000515694.4:n.2326T>A
ENST00000625860.2:c.111T>A ENSP00000486614.1:p.Val37=
ENST00000632775.1:n.794T>A
NM_000668.5:c.231T>A NP_000659.2:p.Val77=
NM_001286650.1:c.111T>A NP_001273579.1:p.Val37=
NM_000668.6:c.231T>A MANE Select NP_000659.2:p.Val77=
NM_001286650.2:c.111T>A NP_001273579.1:p.Val37=