Canonical Allele Identifier: CA2002576362
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442751_116442758delinsCATCCAGT , CM000673.2:g.116442751_116442758delinsCATCCAGT GRCh38
NC_000011.9:g.116313468_116313475delinsCATCCAGT , CM000673.1:g.116313468_116313475delinsCATCCAGT GRCh37
NC_000011.8:g.115818678_115818685delinsCATCCAGT NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748403.1:n.349+31119_349+31126delinsACTGGATG
Search 100 bp 5'
Search 100 bp 3'