Canonical Allele Identifier: CA101653737

Gene: ADH1B

Linked Data

• dbSNP Id: rs141994815
• gnomAD v3: 4-99321860-A-T
• gnomAD v4: 4-99321860-A-T
• MyVariant Identifiers: chr4:g.100243017A>T (hg19) ; chr4:g.99321860A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321860A>T , CM000666.2:g.99321860A>T	GRCh38
NC_000004.11:g.100243017A>T , CM000666.1:g.100243017A>T	GRCh37
NC_000004.10:g.100462040A>T	NCBI36
NG_011435.1:g.4556T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000639454.1:c.19-2974T>A	ENSP00000491622.1:n.19-2974T>A