Canonical Allele Identifier: CA780908298
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1275281063
gnomAD v3: 18-58449999-C-T
gnomAD v4: 18-58449999-C-T
MyVariant Identifiers: chr18:g.56117231C>T (hg19) chr18:g.58449999C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449999C>T , CM000680.2:g.58449999C>T GRCh38
NC_000018.9:g.56117231C>T , CM000680.1:g.56117231C>T GRCh37
NC_000018.8:g.54268211C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1238C>T
NR_170243.1:n.307+459C>T
NR_170244.1:n.307+459C>T
NR_170245.1:n.307+459C>T
Search 100 bp 5'
Search 100 bp 3'