Canonical Allele Identifier: CA2499216386

Gene:

Linked Data

• ClinVar Variation Id: 997764
• ClinVar RCV Id: RCV001293321

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10148440_10158273del , CM000665.2:g.10148440_10158273del	GRCh38
NC_000003.11:g.10190124_10199957del , CM000665.1:g.10190124_10199957del	GRCh37
NC_000003.10:g.10165124_10174957del	NCBI36