Canonical Allele Identifier: CA2306457335
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449962C= , CM000680.2:g.58449962C= GRCh38
NC_000018.9:g.56117194C= , CM000680.1:g.56117194C= GRCh37
NC_000018.8:g.54268174C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1201C=
NR_170243.1:n.307+422C=
NR_170244.1:n.307+422C=
NR_170245.1:n.307+422C=