Canonical Allele Identifier: CA504024867
Gene: MIR122HG HGNC NCBI

Linked Data

gnomAD v4: 18-58449593-C-T
MyVariant Identifiers: chr18:g.56116825C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449593C>T , CM000680.2:g.58449593C>T GRCh38
NC_000018.9:g.56116825C>T , CM000680.1:g.56116825C>T GRCh37
NC_000018.8:g.54267805C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.832C>T
NR_170243.1:n.307+53C>T
NR_170244.1:n.307+53C>T
NR_170245.1:n.307+53C>T
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