Canonical Allele Identifier: CA1479942173
Gene: ADH1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307825G= , CM000666.2:g.99307825G= GRCh38
NC_000004.11:g.100228982G= , CM000666.1:g.100228982G= GRCh37
NC_000004.10:g.100448005G= NCBI36
NG_011435.1:g.18591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*15C= MANE Select ENSP00000306606.8:n.*15C=
ENST00000305046.12:c.*15C= ENSP00000306606.8:n.*15C=
ENST00000506651.5:c.*15C= ENSP00000425998.2:n.*15C=
ENST00000515694.4:n.3238C=
ENST00000625860.2:c.*15C= ENSP00000486614.1:n.*15C=
NM_000668.5:c.*15C= NP_000659.2:n.*15C=
NM_001286650.1:c.*15C= NP_001273579.1:n.*15C=
NM_000668.6:c.*15C= MANE Select NP_000659.2:n.*15C=
NM_001286650.2:c.*15C= NP_001273579.1:n.*15C=
Search 100 bp 5'
Search 100 bp 3'