Canonical Allele Identifier: CA2306457155
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449526T= , CM000680.2:g.58449526T= GRCh38
NC_000018.9:g.56116758T= , CM000680.1:g.56116758T= GRCh37
NC_000018.8:g.54267738T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.765T=
NR_170243.1:n.293T=
NR_170244.1:n.293T=
NR_170245.1:n.293T=