Canonical Allele Identifier: CA780908315
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1394833637
MyVariant Identifiers: chr18:g.56117256G>C (hg19) chr18:g.58450024G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450024G>C , CM000680.2:g.58450024G>C GRCh38
NC_000018.9:g.56117256G>C , CM000680.1:g.56117256G>C GRCh37
NC_000018.8:g.54268236G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1263G>C
NR_170243.1:n.308-467G>C
NR_170244.1:n.307+484G>C
NR_170245.1:n.307+484G>C
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