Canonical Allele Identifier: CA322757483

Gene:

Linked Data

• ClinVar Variation Id: 1267330
• ClinVar RCV Id: RCV001677355
• dbSNP Id: rs374222410
• gnomAD v2: 22-25627870-G-GGT
• gnomAD v3: 22-25231903-G-GGT
• gnomAD v4: 22-25231903-G-GGT
• MyVariant Identifiers: chr22:g.25627872_25627873insGT (hg19) ; chr22:g.25627870_25627871insGT (hg19) ; chr22:g.25231905_25231906insGT (hg38) ; chr22:g.25231903_25231904insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231931_25231932dup , CM000684.2:g.25231931_25231932dup	GRCh38
NC_000022.10:g.25627898_25627899dup , CM000684.1:g.25627898_25627899dup	GRCh37
NC_000022.9:g.23957898_23957899dup	NCBI36
NG_009827.1:g.17287_17288dup