Canonical Allele Identifier: CA2306457393
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051158976

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450074_58450075insC , CM000680.2:g.58450074_58450075insC GRCh38
NC_000018.9:g.56117306_56117307insC , CM000680.1:g.56117306_56117307insC GRCh37
NC_000018.8:g.54268286_54268287insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1313_1314insC
NR_170243.1:n.308-417_308-416insC
NR_170244.1:n.307+534_307+535insC
NR_170245.1:n.307+534_307+535insC