Canonical Allele Identifier: CA300903420
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs546319378
gnomAD v2: 18-56117053-G-A
gnomAD v3: 18-58449821-G-A
gnomAD v4: 18-58449821-G-A
MyVariant Identifiers: chr18:g.56117053G>A (hg19) chr18:g.58449821G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449821G>A , CM000680.2:g.58449821G>A GRCh38
NC_000018.9:g.56117053G>A , CM000680.1:g.56117053G>A GRCh37
NC_000018.8:g.54268033G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1060G>A
NR_170243.1:n.307+281G>A
NR_170244.1:n.307+281G>A
NR_170245.1:n.307+281G>A
Search 100 bp 5'
Search 100 bp 3'