Canonical Allele Identifier: CA2306457187
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051155955

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449636G>C , CM000680.2:g.58449636G>C GRCh38
NC_000018.9:g.56116868G>C , CM000680.1:g.56116868G>C GRCh37
NC_000018.8:g.54267848G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.875G>C
NR_170243.1:n.307+96G>C
NR_170244.1:n.307+96G>C
NR_170245.1:n.307+96G>C