Canonical Allele Identifier: CA780908431
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1305372379
gnomAD v3: 18-58450099-A-G
gnomAD v4: 18-58450099-A-G
MyVariant Identifiers: chr18:g.56117331A>G (hg19) chr18:g.58450099A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58450099A>G , CM000680.2:g.58450099A>G GRCh38
NC_000018.9:g.56117331A>G , CM000680.1:g.56117331A>G GRCh37
NC_000018.8:g.54268311A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.1338A>G
NR_170243.1:n.308-392A>G
NR_170244.1:n.307+559A>G
NR_170245.1:n.307+559A>G
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