Canonical Allele Identifier: CA780908394
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs10605417
gnomAD v3: 18-58450068-A-ATT
gnomAD v4: 18-58450068-A-ATT
MyVariant Identifiers: chr18:g.56117300_56117301insTT (hg19) chr18:g.58450068_58450069insTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450083_58450084dup , CM000680.2:g.58450083_58450084dup GRCh38
NC_000018.9:g.56117315_56117316dup , CM000680.1:g.56117315_56117316dup GRCh37
NC_000018.8:g.54268295_54268296dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1322_1323dup
NR_170243.1:n.308-408_308-407dup
NR_170244.1:n.307+543_307+544dup
NR_170245.1:n.307+543_307+544dup
Search 100 bp 5'
Search 100 bp 3'