Canonical Allele Identifier: CA2136398911
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856990_50856993delinsCCTT , CM000676.2:g.50856990_50856993delinsCCTT GRCh38
NC_000014.8:g.51323708_51323711delinsCCTT , CM000676.1:g.51323708_51323711delinsCCTT GRCh37
NC_000014.7:g.50393458_50393461delinsCCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1105_282+1108delinsAAGG
XR_943848.2:n.643+1105_643+1108delinsAAGG
Search 100 bp 5'
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