Canonical Allele Identifier: CA2529396184
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449683C>T , CM000680.2:g.58449683C>T GRCh38
NC_000018.9:g.56116915C>T , CM000680.1:g.56116915C>T GRCh37
NC_000018.8:g.54267895C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.922C>T
NR_170243.1:n.307+143C>T
NR_170244.1:n.307+143C>T
NR_170245.1:n.307+143C>T