Canonical Allele Identifier: CA780908413
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1187014776
gnomAD v4: 18-58450083-TTC-T
MyVariant Identifiers: chr18:g.56117316_56117317del (hg19) chr18:g.58450084_58450085del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450085_58450086del , CM000680.2:g.58450085_58450086del GRCh38
NC_000018.9:g.56117317_56117318del , CM000680.1:g.56117317_56117318del GRCh37
NC_000018.8:g.54268297_54268298del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1324_1325del
NR_170243.1:n.308-406_308-405del
NR_170244.1:n.307+545_307+546del
NR_170245.1:n.307+545_307+546del
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