Canonical Allele Identifier: CA1479942101
Gene: ADH1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307654C= , CM000666.2:g.99307654C= GRCh38
NC_000004.11:g.100228811C= , CM000666.1:g.100228811C= GRCh37
NC_000004.10:g.100447834C= NCBI36
NG_011435.1:g.18762G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*186G= MANE Select ENSP00000306606.8:n.*186G=
ENST00000305046.12:c.*186G= ENSP00000306606.8:n.*186G=
ENST00000506651.5:c.*186G= ENSP00000425998.2:n.*186G=
ENST00000515694.4:n.3409G=
ENST00000625860.2:c.*186G= ENSP00000486614.1:n.*186G=
NM_000668.5:c.*186G= NP_000659.2:n.*186G=
NM_001286650.1:c.*186G= NP_001273579.1:n.*186G=
NM_000668.6:c.*186G= MANE Select NP_000659.2:n.*186G=
NM_001286650.2:c.*186G= NP_001273579.1:n.*186G=
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