Canonical Allele Identifier: CA10576166

Gene:

Linked Data

• ClinVar Variation Id: 225947
• ClinVar RCV Id: RCV000211190
• dbSNP Id: rs12777823
• gnomAD v2: 10-96405502-G-A
• gnomAD v3: 10-94645745-G-A
• gnomAD v4: 10-94645745-G-A
• MyVariant Identifiers: chr10:g.96405502G>A (hg19) ; chr10:g.94645745G>A (hg38)
• PubMed: PMID:22992668 ; PMID:23755828 ; PMID:25461246 ; PMID:26024874

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94645745G>A , CM000672.2:g.94645745G>A	GRCh38
NC_000010.10:g.96405502G>A , CM000672.1:g.96405502G>A	GRCh37
NC_000010.9:g.96395492G>A	NCBI36