Canonical Allele Identifier: CA947972590
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v3: 12-56041722-A-AGGGGGGAGGGGGGCGG
gnomAD v4: 12-56041722-A-AGGGGGGAGGGGGGCGG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041730_56041731insGGGGGCGGGGGGGGAG , CM000674.2:g.56041730_56041731insGGGGGCGGGGGGGGAG GRCh38
NC_000012.11:g.56435514_56435515insGGGGGCGGGGGGGGAG , CM000674.1:g.56435514_56435515insGGGGGCGGGGGGGGAG GRCh37
NC_000012.10:g.54721781_54721782insGGGGGCGGGGGGGGAG NCBI36
NG_023201.1:g.4829_4830insGGGGGCGGGGGGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-81_-356-80insGGGGGCGGGGGGGGAG ENSP00000348849.5:n.-356-81_-356-80insGGGGGCGGGGGGGGAG
XR_944989.3:n.281_282insCCGCCCCCCTCCCCCC
XR_944990.3:n.281_282insCCGCCCCCCTCCCCCC
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