Canonical Allele Identifier: CA658821624

Gene:

Linked Data

• ClinVar Variation Id: 550538
• ClinVar RCV Id: RCV000665309
• dbSNP Id: rs1587920033
• MyVariant Identifiers: chr9:g.35658089_35658091del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658090_35658092del , CM000671.2:g.35658090_35658092del	GRCh38
NC_000009.11:g.35658087_35658089del , CM000671.1:g.35658087_35658089del	GRCh37
NC_000009.10:g.35648087_35648089del	NCBI36
NG_017041.1:g.4928_4930del , LRG_163:g.4928_4930del
NG_033120.1:g.4801_4803del