Canonical Allele Identifier: CA2306457410
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051159258

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450097G>C , CM000680.2:g.58450097G>C GRCh38
NC_000018.9:g.56117329G>C , CM000680.1:g.56117329G>C GRCh37
NC_000018.8:g.54268309G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1336G>C
NR_170243.1:n.308-394G>C
NR_170244.1:n.307+557G>C
NR_170245.1:n.307+557G>C