Canonical Allele Identifier: CA587570192

Gene:

Linked Data

• ClinVar Variation Id: 554533
• ClinVar RCV Id: RCV000810110 ; RCV000670190
• dbSNP Id: rs1554651404
• gnomAD v2: 9-35658016-A-ACGTCCTCAGCTTCACAGAG
• gnomAD v4: 9-35658019-A-ACGTCCTCAGCTTCACAGAG
• MyVariant Identifiers: chr9:g.35658016_35658017insCGTCCTCAGCTTCACAGAG (hg19) ; chr9:g.35658020_35658038dup (hg38) ; chr9:g.35658019_35658020insCGTCCTCAGCTTCACAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658020_35658038dup , CM000671.2:g.35658020_35658038dup	GRCh38
NC_000009.11:g.35658017_35658035dup , CM000671.1:g.35658017_35658035dup	GRCh37
NC_000009.10:g.35648017_35648035dup	NCBI36
NG_017041.1:g.4981_4999dup , LRG_163:g.4981_4999dup
NG_033120.1:g.4731_4749dup