Canonical Allele Identifier: CA780908415
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1248874398
gnomAD v3: 18-58450084-TC-T
gnomAD v4: 18-58450084-TC-T
MyVariant Identifiers: chr18:g.56117317del (hg19) chr18:g.58450085del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450085del , CM000680.2:g.58450085del GRCh38
NC_000018.9:g.56117317del , CM000680.1:g.56117317del GRCh37
NC_000018.8:g.54268297del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1324del
NR_170243.1:n.308-406del
NR_170244.1:n.307+545del
NR_170245.1:n.307+545del
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