Canonical Allele Identifier: CA504024687
Gene: MIR122HG HGNC NCBI

Linked Data

gnomAD v4: 18-58449562-T-A
MyVariant Identifiers: chr18:g.56116794T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449562T>A , CM000680.2:g.58449562T>A GRCh38
NC_000018.9:g.56116794T>A , CM000680.1:g.56116794T>A GRCh37
NC_000018.8:g.54267774T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.801T>A
NR_170243.1:n.307+22T>A
NR_170244.1:n.307+22T>A
NR_170245.1:n.307+22T>A
Search 100 bp 5'
Search 100 bp 3'