Canonical Allele Identifier: CA2641974794
Gene: MIR122HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449667T>C , CM000680.2:g.58449667T>C GRCh38
NC_000018.9:g.56116899T>C , CM000680.1:g.56116899T>C GRCh37
NC_000018.8:g.54267879T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.906T>C
NR_170243.1:n.307+127T>C
NR_170244.1:n.307+127T>C
NR_170245.1:n.307+127T>C