Canonical Allele Identifier: CA990758715
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051157174

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449817G>A , CM000680.2:g.58449817G>A GRCh38
NC_000018.9:g.56117049G>A , CM000680.1:g.56117049G>A GRCh37
NC_000018.8:g.54268029G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1056G>A
NR_170243.1:n.307+277G>A
NR_170244.1:n.307+277G>A
NR_170245.1:n.307+277G>A