Canonical Allele Identifier: CA2306457158
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449532A= , CM000680.2:g.58449532A= GRCh38
NC_000018.9:g.56116764A= , CM000680.1:g.56116764A= GRCh37
NC_000018.8:g.54267744A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.771A=
NR_170243.1:n.299A=
NR_170244.1:n.299A=
NR_170245.1:n.299A=