Canonical Allele Identifier: CA300903414
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs983117898

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449814C>T , CM000680.2:g.58449814C>T GRCh38
NC_000018.9:g.56117046C>T , CM000680.1:g.56117046C>T GRCh37
NC_000018.8:g.54268026C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1053C>T
NR_170243.1:n.307+274C>T
NR_170244.1:n.307+274C>T
NR_170245.1:n.307+274C>T