Canonical Allele Identifier: CA587570191

Gene:

Linked Data

• ClinVar Variation Id: 555121
• ClinVar RCV Id: RCV000670874 ; RCV001243700
• dbSNP Id: rs1554651403
• gnomAD v2: 9-35658016-A-ACGTCCTCAGCTTCACAGAGT
• gnomAD v3: 9-35658019-A-ACGTCCTCAGCTTCACAGAGT
• gnomAD v4: 9-35658019-A-ACGTCCTCAGCTTCACAGAGT
• MyVariant Identifiers: chr9:g.35658016_35658017insCGTCCTCAGCTTCACAGAGT (hg19) ; chr9:g.35658020_35658039dup (hg38) ; chr9:g.35658019_35658020insCGTCCTCAGCTTCACAGAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658020_35658039dup , CM000671.2:g.35658020_35658039dup	GRCh38
NC_000009.11:g.35658017_35658036dup , CM000671.1:g.35658017_35658036dup	GRCh37
NC_000009.10:g.35648017_35648036dup	NCBI36
NG_017041.1:g.4980_4999dup , LRG_163:g.4980_4999dup
NG_033120.1:g.4731_4750dup