Canonical Allele Identifier: CA910080399

Gene:

Linked Data

• dbSNP Id: rs1329408369
• MyVariant Identifiers: chr3:g.72315928_72315929insGCCATCCTCTAGCTCCTCAGC (hg19) ; chr3:g.72266777_72266778insGCCATCCTCTAGCTCCTCAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266778_72266798dup , CM000665.2:g.72266778_72266798dup	GRCh38
NC_000003.11:g.72315929_72315949dup , CM000665.1:g.72315929_72315949dup	GRCh37
NC_000003.10:g.72398619_72398639dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8310_835+8330dup