Canonical Allele Identifier: CA2735139242
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2144062165

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449838A>G , CM000680.2:g.58449838A>G GRCh38
NC_000018.9:g.56117070A>G , CM000680.1:g.56117070A>G GRCh37
NC_000018.8:g.54268050A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1077A>G
NR_170243.1:n.307+298A>G
NR_170244.1:n.307+298A>G
NR_170245.1:n.307+298A>G