Canonical Allele Identifier: CA2306457169
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449561T= , CM000680.2:g.58449561T= GRCh38
NC_000018.9:g.56116793T= , CM000680.1:g.56116793T= GRCh37
NC_000018.8:g.54267773T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.800T=
NR_170243.1:n.307+21T=
NR_170244.1:n.307+21T=
NR_170245.1:n.307+21T=