Canonical Allele Identifier: CA1479942110
Gene: ADH1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307691C= , CM000666.2:g.99307691C= GRCh38
NC_000004.11:g.100228848C= , CM000666.1:g.100228848C= GRCh37
NC_000004.10:g.100447871C= NCBI36
NG_011435.1:g.18725G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*149G= MANE Select ENSP00000306606.8:n.*149G=
ENST00000305046.12:c.*149G= ENSP00000306606.8:n.*149G=
ENST00000506651.5:c.*149G= ENSP00000425998.2:n.*149G=
ENST00000515694.4:n.3372G=
ENST00000625860.2:c.*149G= ENSP00000486614.1:n.*149G=
NM_000668.5:c.*149G= NP_000659.2:n.*149G=
NM_001286650.1:c.*149G= NP_001273579.1:n.*149G=
NM_000668.6:c.*149G= MANE Select NP_000659.2:n.*149G=
NM_001286650.2:c.*149G= NP_001273579.1:n.*149G=
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