Canonical Allele Identifier: CA340670

Gene:

Linked Data

• ClinVar Variation Id: 7319
• ClinVar RCV Id: RCV000007743
• dbSNP Id: rs1553915517
• MyVariant Identifiers: chr3:g.169481655_169482475del (hg19) ; chr3:g.169763867_169764687del (hg38)
• PubMed: PMID:11574891 ; PMID:20301779

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169763867_169764687del , CM000665.2:g.169763867_169764687del	GRCh38
NC_000003.11:g.169481655_169482475del , CM000665.1:g.169481655_169482475del	GRCh37
NC_000003.10:g.170964349_170965169del	NCBI36
NG_016363.1:g.5378_6198del , LRG_347:g.5378_6198del