Canonical Allele Identifier: CA440300563
Gene: ADH1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100239234A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318077A>G , CM000666.2:g.99318077A>G GRCh38
NC_000004.11:g.100239234A>G , CM000666.1:g.100239234A>G GRCh37
NC_000004.10:g.100458257A>G NCBI36
NG_011435.1:g.8339T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.228T>C MANE Select ENSP00000306606.8:p.Ser76=
ENST00000639454.1:c.228T>C ENSP00000491622.1:p.Ser76=
ENST00000305046.12:c.228T>C ENSP00000306606.8:p.Ser76=
ENST00000504498.1:n.282T>C
ENST00000506651.5:c.108T>C ENSP00000425998.2:p.Ser36=
ENST00000515694.4:n.2323T>C
ENST00000625860.2:c.108T>C ENSP00000486614.1:p.Ser36=
ENST00000632775.1:n.791T>C
NM_000668.5:c.228T>C NP_000659.2:p.Ser76=
NM_001286650.1:c.108T>C NP_001273579.1:p.Ser36=
NM_000668.6:c.228T>C MANE Select NP_000659.2:p.Ser76=
NM_001286650.2:c.108T>C NP_001273579.1:p.Ser36=