Canonical Allele Identifier: CA101653738

Gene: ADH1B

Linked Data

• dbSNP Id: rs971435338
• gnomAD v2: 4-100243046-G-A
• gnomAD v3: 4-99321889-G-A
• gnomAD v4: 4-99321889-G-A
• MyVariant Identifiers: chr4:g.100243046G>A (hg19) ; chr4:g.99321889G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321889G>A , CM000666.2:g.99321889G>A	GRCh38
NC_000004.11:g.100243046G>A , CM000666.1:g.100243046G>A	GRCh37
NC_000004.10:g.100462069G>A	NCBI36
NG_011435.1:g.4527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-3003C>T	ENSP00000491622.1:n.19-3003C>T