Canonical Allele Identifier: CA990758773

Gene: MIR122HG

Linked Data

• dbSNP Id: rs2051157843
• gnomAD v3: 18-58449935-G-GCAAAGAAAAAGAGGCAAATCCAC
• gnomAD v4: 18-58449935-G-GCAAAGAAAAAGAGGCAAATCCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58449935_58449936insCAAAGAAAAAGAGGCAAATCCAC , CM000680.2:g.58449935_58449936insCAAAGAAAAAGAGGCAAATCCAC	GRCh38
NC_000018.9:g.56117167_56117168insCAAAGAAAAAGAGGCAAATCCAC , CM000680.1:g.56117167_56117168insCAAAGAAAAAGAGGCAAATCCAC	GRCh37
NC_000018.8:g.54268147_54268148insCAAAGAAAAAGAGGCAAATCCAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001753465.2:n.1174_1175insCAAAGAAAAAGAGGCAAATCCAC
NR_170243.1:n.307+395_307+396insCAAAGAAAAAGAGGCAAATCCAC
NR_170244.1:n.307+395_307+396insCAAAGAAAAAGAGGCAAATCCAC
NR_170245.1:n.307+395_307+396insCAAAGAAAAAGAGGCAAATCCAC