Canonical Allele Identifier: CA504024650
Gene: MIR122HG HGNC NCBI

Linked Data

gnomAD v4: 18-58449555-T-C
MyVariant Identifiers: chr18:g.56116787T>C (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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