Canonical Allele Identifier: CA2499222419

Gene:

Linked Data

• ClinVar Variation Id: 995907
• ClinVar RCV Id: RCV001523843
• dbSNP Id: rs2138025895

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303707_48303724del , CM000675.2:g.48303707_48303724del	GRCh38
NC_000013.10:g.48877843_48877860del , CM000675.1:g.48877843_48877860del	GRCh37
NC_000013.9:g.47775844_47775861del	NCBI36
NG_009009.1:g.4961_4978del , LRG_517:g.4961_4978del