Canonical Allele Identifier: CA504024355
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116739T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449507T>A , CM000680.2:g.58449507T>A GRCh38
NC_000018.9:g.56116739T>A , CM000680.1:g.56116739T>A GRCh37
NC_000018.8:g.54267719T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.746T>A
NR_170243.1:n.274T>A
NR_170244.1:n.274T>A
NR_170245.1:n.274T>A