Canonical Allele Identifier: CA504025039
Gene: MIR122HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56116856G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449624G>C , CM000680.2:g.58449624G>C GRCh38
NC_000018.9:g.56116856G>C , CM000680.1:g.56116856G>C GRCh37
NC_000018.8:g.54267836G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.863G>C
NR_170243.1:n.307+84G>C
NR_170244.1:n.307+84G>C
NR_170245.1:n.307+84G>C