Canonical Allele Identifier: CA300903485
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs3834611
gnomAD v2: 18-56117171-G-GA
gnomAD v3: 18-58449939-G-GA
gnomAD v4: 18-58449939-G-GA
MyVariant Identifiers: chr18:g.56117171_56117172insA (hg19) chr18:g.58449939_58449940insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449946dup , CM000680.2:g.58449946dup GRCh38
NC_000018.9:g.56117178dup , CM000680.1:g.56117178dup GRCh37
NC_000018.8:g.54268158dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1185dup
NR_170243.1:n.307+406dup
NR_170244.1:n.307+406dup
NR_170245.1:n.307+406dup
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