Canonical Allele Identifier: CA2499220996

Gene:

Linked Data

• ClinVar Variation Id: 1048666
• ClinVar RCV Id: RCV001353256

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5224303_5227790del , CM000673.2:g.5224303_5227790del	GRCh38
NC_000011.9:g.5245533_5249020del , CM000673.1:g.5245533_5249020del	GRCh37
NC_000011.8:g.5202109_5205596del	NCBI36
NG_000007.3:g.69826_73313del
NG_059281.1:g.4282_7769del