Canonical Allele Identifier: CA648883275
Gene: ADH1B HGNC NCBI

Linked Data

COSMIC: COSN23060658
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307808_99307809insC , CM000666.2:g.99307808_99307809insC GRCh38
NC_000004.11:g.100228965_100228966insC , CM000666.1:g.100228965_100228966insC GRCh37
NC_000004.10:g.100447988_100447989insC NCBI36
NG_011435.1:g.18607_18608insG

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.*31_*32insG MANE Select ENSP00000306606.8:n.*31_*32insG
ENST00000305046.12:c.*31_*32insG ENSP00000306606.8:n.*31_*32insG
ENST00000506651.5:c.*31_*32insG ENSP00000425998.2:n.*31_*32insG
ENST00000515694.4:n.3254_3255insG
ENST00000625860.2:c.*31_*32insG ENSP00000486614.1:n.*31_*32insG
NM_000668.5:c.*31_*32insG NP_000659.2:n.*31_*32insG
NM_001286650.1:c.*31_*32insG NP_001273579.1:n.*31_*32insG
NM_000668.6:c.*31_*32insG MANE Select NP_000659.2:n.*31_*32insG
NM_001286650.2:c.*31_*32insG NP_001273579.1:n.*31_*32insG
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Search 100 bp 3'