Canonical Allele Identifier: CA2306457284
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449847T= , CM000680.2:g.58449847T= GRCh38
NC_000018.9:g.56117079T= , CM000680.1:g.56117079T= GRCh37
NC_000018.8:g.54268059T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1086T=
NR_170243.1:n.307+307T=
NR_170244.1:n.307+307T=
NR_170245.1:n.307+307T=