Canonical Allele Identifier: CA990758781
Gene: MIR122HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449939G>A , CM000680.2:g.58449939G>A GRCh38
NC_000018.9:g.56117171G>A , CM000680.1:g.56117171G>A GRCh37
NC_000018.8:g.54268151G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1178G>A
NR_170243.1:n.307+399G>A
NR_170244.1:n.307+399G>A
NR_170245.1:n.307+399G>A