Canonical Allele Identifier: CA553101605

Gene: ADH1B

Linked Data

• dbSNP Id: rs1292216048
• gnomAD v2: 4-100242964-G-A
• gnomAD v3: 4-99321807-G-A
• gnomAD v4: 4-99321807-G-A
• MyVariant Identifiers: chr4:g.100242964G>A (hg19) ; chr4:g.99321807G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99321807G>A , CM000666.2:g.99321807G>A	GRCh38
NC_000004.11:g.100242964G>A , CM000666.1:g.100242964G>A	GRCh37
NC_000004.10:g.100461987G>A	NCBI36
NG_011435.1:g.4609C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639454.1:c.19-2921C>T	ENSP00000491622.1:n.19-2921C>T