Canonical Allele Identifier: CA101653745

Gene: ADH1B

Linked Data

• dbSNP Id: rs918792064
• MyVariant Identifiers: chr4:g.100243069A>T (hg19) ; chr4:g.99321912A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321912A>T , CM000666.2:g.99321912A>T	GRCh38
NC_000004.11:g.100243069A>T , CM000666.1:g.100243069A>T	GRCh37
NC_000004.10:g.100462092A>T	NCBI36
NG_011435.1:g.4504T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-3026T>A	ENSP00000491622.1:n.19-3026T>A