Canonical Allele Identifier: CA192745757

Gene:

Linked Data

• ClinVar Variation Id: 553151
• ClinVar RCV Id: RCV000668535 ; RCV003758902
• dbSNP Id: rs911564838
• gnomAD v2: 9-35658021-CT-C
• gnomAD v3: 9-35658024-CT-C
• gnomAD v4: 9-35658024-CT-C
• MyVariant Identifiers: chr9:g.35658022del (hg19) ; chr9:g.35658025del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658025del , CM000671.2:g.35658025del	GRCh38
NC_000009.11:g.35658022del , CM000671.1:g.35658022del	GRCh37
NC_000009.10:g.35648022del	NCBI36
NG_017041.1:g.4994del , LRG_163:g.4994del
NG_033120.1:g.4736del