Canonical Allele Identifier: CA504024652
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1602165748
MyVariant Identifiers: chr18:g.56116787T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449555T>G , CM000680.2:g.58449555T>G GRCh38
NC_000018.9:g.56116787T>G , CM000680.1:g.56116787T>G GRCh37
NC_000018.8:g.54267767T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.794T>G
NR_170243.1:n.307+15T>G
NR_170244.1:n.307+15T>G
NR_170245.1:n.307+15T>G
Search 100 bp 5'
Search 100 bp 3'