Canonical Allele Identifier: CA14965136

Gene:

Linked Data

• ClinVar Variation Id: 1182056
• ClinVar RCV Id: RCV001539591
• dbSNP Id: rs6004492
• gnomAD v2: 22-25627900-A-T
• gnomAD v3: 22-25231933-A-T
• gnomAD v4: 22-25231933-A-T
• MyVariant Identifiers: chr22:g.25627900A>T (hg19) ; chr22:g.25231933A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231933A>T , CM000684.2:g.25231933A>T	GRCh38
NC_000022.10:g.25627900A>T , CM000684.1:g.25627900A>T	GRCh37
NC_000022.9:g.23957900A>T	NCBI36
NG_009827.1:g.17289A>T