Canonical Allele Identifier: CA915947449

Gene:

Linked Data

• ClinVar Variation Id: 644867
• ClinVar RCV Id: RCV000798854
• dbSNP Id: rs1587919975

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658075_35658076delinsGC , CM000671.2:g.35658075_35658076delinsGC	GRCh38
NC_000009.11:g.35658072_35658073delinsGC , CM000671.1:g.35658072_35658073delinsGC	GRCh37
NC_000009.10:g.35648072_35648073delinsGC	NCBI36
NG_017041.1:g.4943_4944delinsGC , LRG_163:g.4943_4944delinsGC
NG_033120.1:g.4786_4787delinsGC