Canonical Allele Identifier: CA2306457179
Gene: MIR122HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449613T= , CM000680.2:g.58449613T= GRCh38
NC_000018.9:g.56116845T= , CM000680.1:g.56116845T= GRCh37
NC_000018.8:g.54267825T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.852T=
NR_170243.1:n.307+73T=
NR_170244.1:n.307+73T=
NR_170245.1:n.307+73T=