Canonical Allele Identifier: CA605259157
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v2: 12-56435506-A-AGGGGGGAGGGGGGGGG
gnomAD v3: 12-56041722-A-AGGGGGGAGGGGGGGGG
gnomAD v4: 12-56041722-A-AGGGGGGAGGGGGGGGG
MyVariant Identifiers: chr12:g.56435506_56435507insGGGGGGAGGGGGGGGG (hg19) chr12:g.56041722_56041723insGGGGGGAGGGGGGGGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041730_56041731insGGGGGGGGGGGGGGAG , CM000674.2:g.56041730_56041731insGGGGGGGGGGGGGGAG GRCh38
NC_000012.11:g.56435514_56435515insGGGGGGGGGGGGGGAG , CM000674.1:g.56435514_56435515insGGGGGGGGGGGGGGAG GRCh37
NC_000012.10:g.54721781_54721782insGGGGGGGGGGGGGGAG NCBI36
NG_023201.1:g.4829_4830insGGGGGGGGGGGGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-81_-356-80insGGGGGGGGGGGGGGAG ENSP00000348849.5:n.-356-81_-356-80insGGGGGGGGGGGGGGAG
XR_944989.3:n.281_282insCCCCCCCCCTCCCCCC
XR_944990.3:n.281_282insCCCCCCCCCTCCCCCC
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