Canonical Allele Identifier: CA260522

Gene:

Linked Data

• ClinVar Variation Id: 36721
• ClinVar RCV Id: RCV000030400
• dbSNP Id: rs386134265
• gnomAD v2: 10-43572458-C-CCCCCG
• gnomAD v3: 10-43077010-C-CCCCCG
• gnomAD v4: 10-43077010-C-CCCCCG
• MyVariant Identifiers: chr10:g.43572473_43572477dupGCCCC (hg19) ; chr10:g.43572458_43572459insCCCCG (hg19) ; chr10:g.43077025_43077029dupGCCCC (hg38) ; chr10:g.43077010_43077011insCCCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077025_43077029dup , CM000672.2:g.43077025_43077029dup	GRCh38
NC_000010.10:g.43572473_43572477dup , CM000672.1:g.43572473_43572477dup	GRCh37
NC_000010.9:g.42892479_42892483dup	NCBI36
NG_007489.1:g.4957_4961dup , LRG_518:g.4957_4961dup