Canonical Allele Identifier: CA513894884

Gene:

Linked Data

• ClinVar Variation Id: 1326196
• ClinVar RCV Id: RCV001786257
• dbSNP Id: rs374222410
• gnomAD v2: 22-25627870-G-GGTGTGT
• gnomAD v3: 22-25231903-G-GGTGTGT
• gnomAD v4: 22-25231903-G-GGTGTGT
• MyVariant Identifiers: chr22:g.25627872_25627873insGTGTGT (hg19) ; chr22:g.25627870_25627871insGTGTGT (hg19) ; chr22:g.25231905_25231906insGTGTGT (hg38) ; chr22:g.25231903_25231904insGTGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231927_25231932dup , CM000684.2:g.25231927_25231932dup	GRCh38
NC_000022.10:g.25627894_25627899dup , CM000684.1:g.25627894_25627899dup	GRCh37
NC_000022.9:g.23957894_23957899dup	NCBI36
NG_009827.1:g.17283_17288dup