Canonical Allele Identifier: CA2580616182

Gene:

Linked Data

• ClinVar Variation Id: 1677237
• ClinVar RCV Id: RCV002223095
• dbSNP Id: rs1563907859

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658037_35658038insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA , CM000671.2:g.35658037_35658038insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA	GRCh38
NC_000009.11:g.35658034_35658035insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA , CM000671.1:g.35658034_35658035insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA	GRCh37
NC_000009.10:g.35648034_35648035insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA	NCBI36
NG_017041.1:g.4997_4998insTCTGTGAAGCTGAGGATCTGTGAAGCTGAGGA , LRG_163:g.4997_4998insTCTGTGAAGCTGAGGATCTGTGAAGCTGAGGA
NG_033120.1:g.4748_4749insTCCTCAGCTTCACAGATCCTCAGCTTCACAGA