Canonical Allele Identifier: CA630057318
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1245529625
gnomAD v2: 18-56117305-T-TA
gnomAD v3: 18-58450073-T-TA
gnomAD v4: 18-58450073-T-TA
MyVariant Identifiers: chr18:g.56117305_56117306insA (hg19) chr18:g.58450073_58450074insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450073_58450074insA , CM000680.2:g.58450073_58450074insA GRCh38
NC_000018.9:g.56117305_56117306insA , CM000680.1:g.56117305_56117306insA GRCh37
NC_000018.8:g.54268285_54268286insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1312_1313insA
NR_170243.1:n.308-418_308-417insA
NR_170244.1:n.307+533_307+534insA
NR_170245.1:n.307+533_307+534insA
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