Canonical Allele Identifier: CA504024896
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116830C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449598C>T , CM000680.2:g.58449598C>T GRCh38
NC_000018.9:g.56116830C>T , CM000680.1:g.56116830C>T GRCh37
NC_000018.8:g.54267810C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.837C>T
NR_170243.1:n.307+58C>T
NR_170244.1:n.307+58C>T
NR_170245.1:n.307+58C>T