Canonical Allele Identifier: CA587570183

Gene:

Linked Data

• ClinVar Variation Id: 929121
• ClinVar RCV Id: RCV001194117 ; RCV001244477
• dbSNP Id: rs1563907710
• gnomAD v2: 9-35658014-C-CCACGTCCTCAGCTTCACAGAG
• gnomAD v4: 9-35658017-C-CCACGTCCTCAGCTTCACAGAG
• MyVariant Identifiers: chr9:g.35658014_35658015insCACGTCCTCAGCTTCACAGAG (hg19) ; chr9:g.35658017_35658018insCACGTCCTCAGCTTCACAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658018_35658038dup , CM000671.2:g.35658018_35658038dup	GRCh38
NC_000009.11:g.35658015_35658035dup , CM000671.1:g.35658015_35658035dup	GRCh37
NC_000009.10:g.35648015_35648035dup	NCBI36
NG_017041.1:g.4981_5001dup , LRG_163:g.4981_5001dup
NG_033120.1:g.4729_4749dup