Canonical Allele Identifier: CA322757509

Gene:

Linked Data

• ClinVar Variation Id: 1197239
• ClinVar RCV Id: RCV001560995
• dbSNP Id: rs5760929
• gnomAD v2: 22-25627898-T-A
• gnomAD v3: 22-25231931-T-A
• gnomAD v4: 22-25231931-T-A
• MyVariant Identifiers: chr22:g.25627898T>A (hg19) ; chr22:g.25627898_25627900delinsAGA (hg19) ; chr22:g.25231931T>A (hg38) ; chr22:g.25231931_25231933delinsAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231931T>A , CM000684.2:g.25231931T>A	GRCh38
NC_000022.10:g.25627898T>A , CM000684.1:g.25627898T>A	GRCh37
NC_000022.9:g.23957898T>A	NCBI36
NG_009827.1:g.17287T>A