Canonical Allele Identifier: CA1065904900
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1734038992
gnomAD v3: 4-99321802-A-C
gnomAD v4: 4-99321802-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321802A>C , CM000666.2:g.99321802A>C GRCh38
NC_000004.11:g.100242959A>C , CM000666.1:g.100242959A>C GRCh37
NC_000004.10:g.100461982A>C NCBI36
NG_011435.1:g.4614T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000639454.1:c.19-2916T>G ENSP00000491622.1:n.19-2916T>G