Canonical Allele Identifier: CA504024963
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116843T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449611T>A , CM000680.2:g.58449611T>A GRCh38
NC_000018.9:g.56116843T>A , CM000680.1:g.56116843T>A GRCh37
NC_000018.8:g.54267823T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.850T>A
NR_170243.1:n.307+71T>A
NR_170244.1:n.307+71T>A
NR_170245.1:n.307+71T>A
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