Canonical Allele Identifier: CA440300709
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100239327T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318170T>A , CM000666.2:g.99318170T>A GRCh38
NC_000004.11:g.100239327T>A , CM000666.1:g.100239327T>A GRCh37
NC_000004.10:g.100458350T>A NCBI36
NG_011435.1:g.8246A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.135A>T MANE Select ENSP00000306606.8:p.Gly45=
ENST00000639454.1:c.135A>T ENSP00000491622.1:p.Gly45=
ENST00000305046.12:c.135A>T ENSP00000306606.8:p.Gly45=
ENST00000504498.1:n.189A>T
ENST00000506651.5:c.15A>T ENSP00000425998.2:p.Gly5=
ENST00000515694.4:n.2230A>T
ENST00000625860.2:c.15A>T ENSP00000486614.1:p.Gly5=
ENST00000632775.1:n.698A>T
NM_000668.5:c.135A>T NP_000659.2:p.Gly45=
NM_001286650.1:c.15A>T NP_001273579.1:p.Gly5=
NM_000668.6:c.135A>T MANE Select NP_000659.2:p.Gly45=
NM_001286650.2:c.15A>T NP_001273579.1:p.Gly5=