Canonical Allele Identifier: CA12805641

Gene:

Linked Data

• ClinVar Variation Id: 1276393
• ClinVar RCV Id: RCV001687585
• dbSNP Id: rs7840433
• gnomAD v2: 8-11422170-A-G
• gnomAD v3: 8-11564661-A-G
• gnomAD v4: 8-11564661-A-G
• MyVariant Identifiers: chr8:g.11422170A>G (hg19) ; chr8:g.11564661A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564661A>G , CM000670.2:g.11564661A>G	GRCh38
NC_000008.10:g.11422170A>G , CM000670.1:g.11422170A>G	GRCh37
NC_000008.9:g.11459579A>G	NCBI36
NG_023543.1:g.75650A>G
NG_023543.2:g.75650A>G