Canonical Allele Identifier: CA990758819
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051158438

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450023A>G , CM000680.2:g.58450023A>G GRCh38
NC_000018.9:g.56117255A>G , CM000680.1:g.56117255A>G GRCh37
NC_000018.8:g.54268235A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1262A>G
NR_170243.1:n.308-468A>G
NR_170244.1:n.307+483A>G
NR_170245.1:n.307+483A>G