Canonical Allele Identifier: CA300903701
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs10605417
gnomAD v2: 18-56117300-ATTT-A
gnomAD v3: 18-58450068-ATTT-A
gnomAD v4: 18-58450068-ATTT-A
MyVariant Identifiers: chr18:g.56117302_56117304del (hg19) chr18:g.56117301_56117303del (hg19) chr18:g.58450070_58450072del (hg38) chr18:g.58450069_58450071del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450082_58450084del , CM000680.2:g.58450082_58450084del GRCh38
NC_000018.9:g.56117314_56117316del , CM000680.1:g.56117314_56117316del GRCh37
NC_000018.8:g.54268294_54268296del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1321_1323del
NR_170243.1:n.308-409_308-407del
NR_170244.1:n.307+542_307+544del
NR_170245.1:n.307+542_307+544del
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