Canonical Allele Identifier: CA800706456
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs1356163190
MyVariant Identifiers: chr4:g.100242905T>A (hg19) chr4:g.99321748T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321748T>A , CM000666.2:g.99321748T>A GRCh38
NC_000004.11:g.100242905T>A , CM000666.1:g.100242905T>A GRCh37
NC_000004.10:g.100461928T>A NCBI36
NG_011435.1:g.4668A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000639454.1:c.19-2862A>T ENSP00000491622.1:n.19-2862A>T
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