Canonical Allele Identifier: CA2499216339

Gene:

Linked Data

• ClinVar Variation Id: 997740
• ClinVar RCV Id: RCV001293297

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10135142_10143568del , CM000665.2:g.10135142_10143568del	GRCh38
NC_000003.11:g.10176826_10185252del , CM000665.1:g.10176826_10185252del	GRCh37
NC_000003.10:g.10151826_10160252del	NCBI36