Canonical Allele Identifier: CA504024338
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116737T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449505T>G , CM000680.2:g.58449505T>G GRCh38
NC_000018.9:g.56116737T>G , CM000680.1:g.56116737T>G GRCh37
NC_000018.8:g.54267717T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.744T>G
NR_170243.1:n.272T>G
NR_170244.1:n.272T>G
NR_170245.1:n.272T>G