Canonical Allele Identifier: CA1479946652
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1733927809
gnomAD v4: 4-99318028-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99318028T>C , CM000666.2:g.99318028T>C GRCh38
NC_000004.11:g.100239185T>C , CM000666.1:g.100239185T>C GRCh37
NC_000004.10:g.100458208T>C NCBI36
NG_011435.1:g.8388A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305046.13:c.259+18A>G MANE Select ENSP00000306606.8:n.259+18A>G
ENST00000639454.1:c.259+18A>G ENSP00000491622.1:n.259+18A>G
ENST00000305046.12:c.259+18A>G ENSP00000306606.8:n.259+18A>G
ENST00000504498.1:n.331A>G
ENST00000506651.5:c.139+18A>G ENSP00000425998.2:n.139+18A>G
ENST00000515694.4:n.2354+18A>G
ENST00000625860.2:c.139+18A>G ENSP00000486614.1:n.139+18A>G
ENST00000632775.1:n.840A>G
NM_000668.5:c.259+18A>G NP_000659.2:n.259+18A>G
NM_001286650.1:c.139+18A>G NP_001273579.1:n.139+18A>G
NM_000668.6:c.259+18A>G MANE Select NP_000659.2:n.259+18A>G
NM_001286650.2:c.139+18A>G NP_001273579.1:n.139+18A>G