Canonical Allele Identifier: CA2735139217
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2144061818

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449625C>A , CM000680.2:g.58449625C>A GRCh38
NC_000018.9:g.56116857C>A , CM000680.1:g.56116857C>A GRCh37
NC_000018.8:g.54267837C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.864C>A
NR_170243.1:n.307+85C>A
NR_170244.1:n.307+85C>A
NR_170245.1:n.307+85C>A