Canonical Allele Identifier: CA2306457361
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450029A= , CM000680.2:g.58450029A= GRCh38
NC_000018.9:g.56117261A= , CM000680.1:g.56117261A= GRCh37
NC_000018.8:g.54268241A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1268A=
NR_170243.1:n.308-462A=
NR_170244.1:n.307+489A=
NR_170245.1:n.307+489A=