Canonical Allele Identifier: CA101653721

Gene: ADH1B

Linked Data

• dbSNP Id: rs911664922
• MyVariant Identifiers: chr4:g.100242979C>T (hg19) ; chr4:g.99321822C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321822C>T , CM000666.2:g.99321822C>T	GRCh38
NC_000004.11:g.100242979C>T , CM000666.1:g.100242979C>T	GRCh37
NC_000004.10:g.100462002C>T	NCBI36
NG_011435.1:g.4594G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-2936G>A	ENSP00000491622.1:n.19-2936G>A