Canonical Allele Identifier: CA5045868

Gene:

Linked Data

• ClinVar Variation Id: 933554
• ClinVar RCV Id: RCV001201791
• dbSNP Id: rs1554651349
• ExAC: 9:35658010 C / CGAACCACGTCCTCAGCTTCACAGAGTAG
• gnomAD v2: 9-35658010-C-CGAACCACGTCCTCAGCTTCACAGAGTAG
• gnomAD v4: 9-35658013-C-CGAACCACGTCCTCAGCTTCACAGAGTAG
• MyVariant Identifiers: chr9:g.35658010_35658011insGAACCACGTCCTCAGCTTCACAGAGTAG (hg19) ; chr9:g.35658013_35658014insGAACCACGTCCTCAGCTTCACAGAGTAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658014_35658041dup , CM000671.2:g.35658014_35658041dup	GRCh38
NC_000009.11:g.35658011_35658038dup , CM000671.1:g.35658011_35658038dup	GRCh37
NC_000009.10:g.35648011_35648038dup	NCBI36
NG_017041.1:g.4978_5005dup , LRG_163:g.4978_5005dup
NG_033120.1:g.4725_4752dup