Canonical Allele Identifier: CA172096188

Gene:

Linked Data

• ClinVar Variation Id: 1326093
• ClinVar RCV Id: RCV001786154
• dbSNP Id: rs144735885
• gnomAD v2: 8-11422277-G-A
• gnomAD v3: 8-11564768-G-A
• gnomAD v4: 8-11564768-G-A
• MyVariant Identifiers: chr8:g.11422277G>A (hg19) ; chr8:g.11564768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564768G>A , CM000670.2:g.11564768G>A	GRCh38
NC_000008.10:g.11422277G>A , CM000670.1:g.11422277G>A	GRCh37
NC_000008.9:g.11459686G>A	NCBI36
NG_023543.1:g.75757G>A
NG_023543.2:g.75757G>A