Canonical Allele Identifier: CA322757502

Gene:

Linked Data

• ClinVar Variation Id: 1221880
• ClinVar RCV Id: RCV001595698
• dbSNP Id: rs374222410
• gnomAD v2: 22-25627870-G-GGTGT
• gnomAD v3: 22-25231903-G-GGTGT
• gnomAD v4: 22-25231903-G-GGTGT
• MyVariant Identifiers: chr22:g.25627899_25627900insTGTG (hg19) ; chr22:g.25627872_25627873insGTGT (hg19) ; chr22:g.25627870_25627871insGTGT (hg19) ; chr22:g.25231932_25231933insTGTG (hg38) ; chr22:g.25231905_25231906insGTGT (hg38) ; chr22:g.25231903_25231904insGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231929_25231932dup , CM000684.2:g.25231929_25231932dup	GRCh38
NC_000022.10:g.25627896_25627899dup , CM000684.1:g.25627896_25627899dup	GRCh37
NC_000022.9:g.23957896_23957899dup	NCBI36
NG_009827.1:g.17285_17288dup