Canonical Allele Identifier: CA2306457207
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051156241

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449670C>T , CM000680.2:g.58449670C>T GRCh38
NC_000018.9:g.56116902C>T , CM000680.1:g.56116902C>T GRCh37
NC_000018.8:g.54267882C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.909C>T
NR_170243.1:n.307+130C>T
NR_170244.1:n.307+130C>T
NR_170245.1:n.307+130C>T