Canonical Allele Identifier: CA2306457198
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449655A= , CM000680.2:g.58449655A= GRCh38
NC_000018.9:g.56116887A= , CM000680.1:g.56116887A= GRCh37
NC_000018.8:g.54267867A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.894A=
NR_170243.1:n.307+115A=
NR_170244.1:n.307+115A=
NR_170245.1:n.307+115A=