Canonical Allele Identifier: CA990758671
Gene: MIR122HG HGNC NCBI

Linked Data

dbSNP Id: rs948359090
gnomAD v3: 18-58449692-T-C
gnomAD v4: 18-58449692-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449692T>C , CM000680.2:g.58449692T>C GRCh38
NC_000018.9:g.56116924T>C , CM000680.1:g.56116924T>C GRCh37
NC_000018.8:g.54267904T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.931T>C
NR_170243.1:n.307+152T>C
NR_170244.1:n.307+152T>C
NR_170245.1:n.307+152T>C
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