Canonical Allele Identifier: CA2306457222
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051156489

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449704G>A , CM000680.2:g.58449704G>A GRCh38
NC_000018.9:g.56116936G>A , CM000680.1:g.56116936G>A GRCh37
NC_000018.8:g.54267916G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.943G>A
NR_170243.1:n.307+164G>A
NR_170244.1:n.307+164G>A
NR_170245.1:n.307+164G>A