Canonical Allele Identifier: CA1479942202
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307883G= , CM000666.2:g.99307883G= GRCh38
NC_000004.11:g.100229040G= , CM000666.1:g.100229040G= GRCh37
NC_000004.10:g.100448063G= NCBI36
NG_011435.1:g.18533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.1104-19C= MANE Select ENSP00000306606.8:n.1104-19C=
ENST00000639454.1:c.1104-19C= ENSP00000491622.1:n.1104-19C=
ENST00000305046.12:c.1104-19C= ENSP00000306606.8:n.1104-19C=
ENST00000506651.5:c.984-19C= ENSP00000425998.2:n.984-19C=
ENST00000515694.4:n.3199-19C=
ENST00000625860.2:c.984-19C= ENSP00000486614.1:n.984-19C=
NM_000668.5:c.1104-19C= NP_000659.2:n.1104-19C=
NM_001286650.1:c.984-19C= NP_001273579.1:n.984-19C=
NM_000668.6:c.1104-19C= MANE Select NP_000659.2:n.1104-19C=
NM_001286650.2:c.984-19C= NP_001273579.1:n.984-19C=