Canonical Allele Identifier: CA658797198

Gene:

Linked Data

• ClinVar Variation Id: 533763
• ClinVar RCV Id: RCV000641008
• dbSNP Id: rs1554651385
• gnomAD v3: 9-35658017-C-CCACGTCCTCAGCTTCACAGAGTAGTAT
• gnomAD v4: 9-35658017-C-CCACGTCCTCAGCTTCACAGAGTAGTAT
• MyVariant Identifiers: chr9:g.35658015_35658041dup (hg19) ; chr9:g.35658018_35658044dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658018_35658044dup , CM000671.2:g.35658018_35658044dup	GRCh38
NC_000009.11:g.35658015_35658041dup , CM000671.1:g.35658015_35658041dup	GRCh37
NC_000009.10:g.35648015_35648041dup	NCBI36
NG_017041.1:g.4975_5001dup , LRG_163:g.4975_5001dup
NG_033120.1:g.4729_4755dup