Canonical Allele Identifier: CA101653644
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1037584854
gnomAD v2: 4-100242816-C-T
gnomAD v3: 4-99321659-C-T
gnomAD v4: 4-99321659-C-T
MyVariant Identifiers: chr4:g.100242816C>T (hg19) chr4:g.100242816_100242818delinsTGG (hg19) chr4:g.99321659C>T (hg38) chr4:g.99321659_99321661delinsTGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321659C>T , CM000666.2:g.99321659C>T GRCh38
NC_000004.11:g.100242816C>T , CM000666.1:g.100242816C>T GRCh37
NC_000004.10:g.100461839C>T NCBI36
NG_011435.1:g.4757G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000639454.1:c.19-2773G>A ENSP00000491622.1:n.19-2773G>A
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