Canonical Allele Identifier: CA1479946727
Gene: ADH1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318186T= , CM000666.2:g.99318186T= GRCh38
NC_000004.11:g.100239343T= , CM000666.1:g.100239343T= GRCh37
NC_000004.10:g.100458366T= NCBI36
NG_011435.1:g.8230A=

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.121-2A= MANE Select ENSP00000306606.8:n.121-2A=
ENST00000639454.1:c.121-2A= ENSP00000491622.1:n.121-2A=
ENST00000305046.12:c.121-2A= ENSP00000306606.8:n.121-2A=
ENST00000504498.1:n.175-2A=
ENST00000506651.5:c.1-2A= ENSP00000425998.2:n.1-2A=
ENST00000515694.4:n.2216-2A=
ENST00000625860.2:c.1-2A= ENSP00000486614.1:n.1-2A=
ENST00000632775.1:n.682A=
NM_000668.5:c.121-2A= NP_000659.2:n.121-2A=
NM_001286650.1:c.1-2A= NP_001273579.1:n.1-2A=
NM_000668.6:c.121-2A= MANE Select NP_000659.2:n.121-2A=
NM_001286650.2:c.1-2A= NP_001273579.1:n.1-2A=