Canonical Allele Identifier: CA440300707
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100239324G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318167G>T , CM000666.2:g.99318167G>T GRCh38
NC_000004.11:g.100239324G>T , CM000666.1:g.100239324G>T GRCh37
NC_000004.10:g.100458347G>T NCBI36
NG_011435.1:g.8249C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.138C>A MANE Select ENSP00000306606.8:p.Ile46=
ENST00000639454.1:c.138C>A ENSP00000491622.1:p.Ile46=
ENST00000305046.12:c.138C>A ENSP00000306606.8:p.Ile46=
ENST00000504498.1:n.192C>A
ENST00000506651.5:c.18C>A ENSP00000425998.2:p.Ile6=
ENST00000515694.4:n.2233C>A
ENST00000625860.2:c.18C>A ENSP00000486614.1:p.Ile6=
ENST00000632775.1:n.701C>A
NM_000668.5:c.138C>A NP_000659.2:p.Ile46=
NM_001286650.1:c.18C>A NP_001273579.1:p.Ile6=
NM_000668.6:c.138C>A MANE Select NP_000659.2:p.Ile46=
NM_001286650.2:c.18C>A NP_001273579.1:p.Ile6=