Canonical Allele Identifier: CA587570180

Gene:

Linked Data

• ClinVar Variation Id: 1373627
• ClinVar RCV Id: RCV001900414
• dbSNP Id: rs1563907676
• gnomAD v2: 9-35658012-A-AACCACGTCCTCAGCTTCACAGAGT
• gnomAD v4: 9-35658015-A-AACCACGTCCTCAGCTTCACAGAGT
• MyVariant Identifiers: chr9:g.35658012_35658013insACCACGTCCTCAGCTTCACAGAGT (hg19) ; chr9:g.35658015_35658016insACCACGTCCTCAGCTTCACAGAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658017_35658040dup , CM000671.2:g.35658017_35658040dup	GRCh38
NC_000009.11:g.35658014_35658037dup , CM000671.1:g.35658014_35658037dup	GRCh37
NC_000009.10:g.35648014_35648037dup	NCBI36
NG_017041.1:g.4980_5003dup , LRG_163:g.4980_5003dup
NG_033120.1:g.4728_4751dup