Canonical Allele Identifier: CA780908410

Gene: MIR122HG

Linked Data

• dbSNP Id: rs1455012148
• MyVariant Identifiers: chr18:g.56117309T>A (hg19) ; chr18:g.58450077T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58450077T>A , CM000680.2:g.58450077T>A	GRCh38
NC_000018.9:g.56117309T>A , CM000680.1:g.56117309T>A	GRCh37
NC_000018.8:g.54268289T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.1316T>A
NR_170243.1:n.308-414T>A
NR_170244.1:n.307+537T>A
NR_170245.1:n.307+537T>A