Canonical Allele Identifier: CA343834

Gene:

Linked Data

• ClinVar Variation Id: 40977
• ClinVar RCV Id: RCV000033869
• MyVariant Identifiers: chr3:g.169482533_169485508del (hg19) ; chr3:g.169764745_169767720del (hg38)
• PubMed: PMID:15098033 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764745_169767720del , CM000665.2:g.169764745_169767720del	GRCh38
NC_000003.11:g.169482533_169485508del , CM000665.1:g.169482533_169485508del	GRCh37
NC_000003.10:g.170965227_170968202del	NCBI36
NG_016363.1:g.2345_5320del , LRG_347:g.2345_5320del