Canonical Allele Identifier: CA2812654597
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449658A>T , CM000680.2:g.58449658A>T GRCh38
NC_000018.9:g.56116890A>T , CM000680.1:g.56116890A>T GRCh37
NC_000018.8:g.54267870A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.897A>T
NR_170243.1:n.307+118A>T
NR_170244.1:n.307+118A>T
NR_170245.1:n.307+118A>T