Canonical Allele Identifier: CA124673

Gene:

Linked Data

• ClinVar Variation Id: 15063
• ClinVar RCV Id: RCV000016213
• MyVariant Identifiers: chr11:g.5248144_5255556del (hg19) ; chr11:g.5226914_5234326del (hg38)
• PubMed: PMID:5660684 ; PMID:14133899 ; PMID:14478740 ; PMID:16114186

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226914_5234326del , CM000673.2:g.5226914_5234326del	GRCh38
NC_000011.9:g.5248144_5255556del , CM000673.1:g.5248144_5255556del	GRCh37
NC_000011.8:g.5204720_5212132del	NCBI36
NG_000007.3:g.63290_70702del