Canonical Allele Identifier: CA1065899721
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1733644990

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307666_99307667insCA , CM000666.2:g.99307666_99307667insCA GRCh38
NC_000004.11:g.100228823_100228824insCA , CM000666.1:g.100228823_100228824insCA GRCh37
NC_000004.10:g.100447846_100447847insCA NCBI36
NG_011435.1:g.18750_18751insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.*174_*175insGT MANE Select ENSP00000306606.8:n.*174_*175insGT
ENST00000305046.12:c.*174_*175insGT ENSP00000306606.8:n.*174_*175insGT
ENST00000506651.5:c.*174_*175insGT ENSP00000425998.2:n.*174_*175insGT
ENST00000515694.4:n.3397_3398insGT
ENST00000625860.2:c.*174_*175insGT ENSP00000486614.1:n.*174_*175insGT
NM_000668.5:c.*174_*175insGT NP_000659.2:n.*174_*175insGT
NM_001286650.1:c.*174_*175insGT NP_001273579.1:n.*174_*175insGT
NM_000668.6:c.*174_*175insGT MANE Select NP_000659.2:n.*174_*175insGT
NM_001286650.2:c.*174_*175insGT NP_001273579.1:n.*174_*175insGT