Canonical Allele Identifier: CA990758768
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051157816
gnomAD v3: 18-58449933-G-GA
gnomAD v4: 18-58449933-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449933_58449934insA , CM000680.2:g.58449933_58449934insA GRCh38
NC_000018.9:g.56117165_56117166insA , CM000680.1:g.56117165_56117166insA GRCh37
NC_000018.8:g.54268145_54268146insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1172_1173insA
NR_170243.1:n.307+393_307+394insA
NR_170244.1:n.307+393_307+394insA
NR_170245.1:n.307+393_307+394insA
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