Canonical Allele Identifier: CA2306457432
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1426061705

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450181C>G , CM000680.2:g.58450181C>G GRCh38
NC_000018.9:g.56117413C>G , CM000680.1:g.56117413C>G GRCh37
NC_000018.8:g.54268393C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1420C>G
NR_170243.1:n.308-310C>G
NR_170244.1:n.307+641C>G
NR_170245.1:n.308-638C>G