Canonical Allele Identifier: CA101653681

Gene: ADH1B

Linked Data

• dbSNP Id: rs1047321667
• gnomAD v3: 4-99321706-G-T
• gnomAD v4: 4-99321706-G-T
• MyVariant Identifiers: chr4:g.99321706G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321706G>T , CM000666.2:g.99321706G>T	GRCh38
NC_000004.11:g.100242863G>T , CM000666.1:g.100242863G>T	GRCh37
NC_000004.10:g.100461886G>T	NCBI36
NG_011435.1:g.4710C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-2820C>A	ENSP00000491622.1:n.19-2820C>A