Canonical Allele Identifier: CA101653689
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs971195113
MyVariant Identifiers: chr4:g.100242879C>T (hg19) chr4:g.99321722C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321722C>T , CM000666.2:g.99321722C>T GRCh38
NC_000004.11:g.100242879C>T , CM000666.1:g.100242879C>T GRCh37
NC_000004.10:g.100461902C>T NCBI36
NG_011435.1:g.4694G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000639454.1:c.19-2836G>A ENSP00000491622.1:n.19-2836G>A
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