Canonical Allele Identifier: CA780908435
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1364099608
MyVariant Identifiers: chr18:g.56117343C>T (hg19) chr18:g.58450111C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450111C>T , CM000680.2:g.58450111C>T GRCh38
NC_000018.9:g.56117343C>T , CM000680.1:g.56117343C>T GRCh37
NC_000018.8:g.54268323C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1350C>T
NR_170243.1:n.308-380C>T
NR_170244.1:n.307+571C>T
NR_170245.1:n.307+571C>T
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