Canonical Allele Identifier: CA504024553
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116770C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449538C>G , CM000680.2:g.58449538C>G GRCh38
NC_000018.9:g.56116770C>G , CM000680.1:g.56116770C>G GRCh37
NC_000018.8:g.54267750C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.777C>G
NR_170243.1:n.305C>G
NR_170244.1:n.305C>G
NR_170245.1:n.305C>G