Canonical Allele Identifier: CA124669

Gene:

Linked Data

• ClinVar Variation Id: 15060
• ClinVar RCV Id: RCV000016207
• MyVariant Identifiers: chr11:g.5247868_5255282del (hg19) ; chr11:g.5226638_5234052del (hg38)
• PubMed: PMID:701081 ; PMID:2442092 ; PMID:5356627

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226638_5234052del , CM000673.2:g.5226638_5234052del	GRCh38
NC_000011.9:g.5247868_5255282del , CM000673.1:g.5247868_5255282del	GRCh37
NC_000011.8:g.5204444_5211858del	NCBI36
NG_000007.3:g.63568_70982del