Canonical Allele Identifier: CA101653749

Gene: ADH1B

Linked Data

• dbSNP Id: rs973820760
• gnomAD v2: 4-100243096-T-G
• gnomAD v3: 4-99321939-T-G
• gnomAD v4: 4-99321939-T-G
• MyVariant Identifiers: chr4:g.100243096T>G (hg19) ; chr4:g.99321939T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321939T>G , CM000666.2:g.99321939T>G	GRCh38
NC_000004.11:g.100243096T>G , CM000666.1:g.100243096T>G	GRCh37
NC_000004.10:g.100462119T>G	NCBI36
NG_011435.1:g.4477A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-3053A>C	ENSP00000491622.1:n.19-3053A>C