Canonical Allele Identifier: CA321283654

Gene:

Linked Data

• ClinVar Variation Id: 1187188
• ClinVar RCV Id: RCV001546549
• dbSNP Id: rs41277574
• gnomAD v2: 22-18560597-T-C
• gnomAD v3: 22-18077831-T-C
• gnomAD v4: 22-18077831-T-C
• MyVariant Identifiers: chr22:g.18560597T>C (hg19) ; chr22:g.18077831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18077831T>C , CM000684.2:g.18077831T>C	GRCh38
NC_000022.10:g.18560597T>C , CM000684.1:g.18560597T>C	GRCh37
NC_000022.9:g.16940597T>C	NCBI36
NG_008339.1:g.4912T>C