Canonical Allele Identifier: CA918446892

Gene:

Linked Data

• ClinVar Variation Id: 1454053
• ClinVar RCV Id: RCV001939396
• dbSNP Id: rs1554651376
• gnomAD v4: 9-35658017-C-CCACGTCCTCAGCTTCACAGAGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658018_35658040dup , CM000671.2:g.35658018_35658040dup	GRCh38
NC_000009.11:g.35658015_35658037dup , CM000671.1:g.35658015_35658037dup	GRCh37
NC_000009.10:g.35648015_35648037dup	NCBI36
NG_017041.1:g.4979_5001dup , LRG_163:g.4979_5001dup
NG_033120.1:g.4729_4751dup