Canonical Allele Identifier: CA212289

Gene:

Linked Data

• ClinVar Variation Id: 157195
• ClinVar RCV Id: RCV000161621
• MyVariant Identifiers: chr11:g.8959020_8964938del (hg19) ; chr11:g.8937473_8943391del (hg38)
• PubMed: PMID:25666259

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8937474_8943392del , CM000673.2:g.8937474_8943392del	GRCh38
NC_000011.9:g.8959021_8964939del , CM000673.1:g.8959021_8964939del	GRCh37
NC_000011.8:g.8915597_8921515del	NCBI36