Canonical Allele Identifier: CA101653684
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs891084912
MyVariant Identifiers: chr4:g.100242864T>A (hg19) chr4:g.99321707T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321707T>A , CM000666.2:g.99321707T>A GRCh38
NC_000004.11:g.100242864T>A , CM000666.1:g.100242864T>A GRCh37
NC_000004.10:g.100461887T>A NCBI36
NG_011435.1:g.4709A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000639454.1:c.19-2821A>T ENSP00000491622.1:n.19-2821A>T
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