Canonical Allele Identifier: CA630396155
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs1470588859
gnomAD v2: 18-56116883-G-C
gnomAD v3: 18-58449651-G-C
gnomAD v4: 18-58449651-G-C
MyVariant Identifiers: chr18:g.56116883G>C (hg19) chr18:g.58449651G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449651G>C , CM000680.2:g.58449651G>C GRCh38
NC_000018.9:g.56116883G>C , CM000680.1:g.56116883G>C GRCh37
NC_000018.8:g.54267863G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.890G>C
NR_170243.1:n.307+111G>C
NR_170244.1:n.307+111G>C
NR_170245.1:n.307+111G>C
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