Canonical Allele Identifier: CA990758908
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs2051159128
gnomAD v3: 18-58450084-TCTG-T
gnomAD v4: 18-58450084-TCTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450085_58450087del , CM000680.2:g.58450085_58450087del GRCh38
NC_000018.9:g.56117317_56117319del , CM000680.1:g.56117317_56117319del GRCh37
NC_000018.8:g.54268297_54268299del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1324_1326del
NR_170243.1:n.308-406_308-404del
NR_170244.1:n.307+545_307+547del
NR_170245.1:n.307+545_307+547del
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