Canonical Allele Identifier: CA35930389

Gene:

Linked Data

• ClinVar Variation Id: 427752
• ClinVar RCV Id: RCV000509072 ; RCV001777165
• dbSNP Id: rs9660525
• gnomAD v2: 1-198776931-C-A
• gnomAD v3: 1-198807802-C-A
• gnomAD v4: 1-198807802-C-A
• MyVariant Identifiers: chr1:g.198776931C>A (hg19) ; chr1:g.198807802C>A (hg38)
• PubMed: PMID:29254171

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198807802C>A , CM000663.2:g.198807802C>A	GRCh38
NC_000001.10:g.198776931C>A , CM000663.1:g.198776931C>A	GRCh37
NC_000001.9:g.197043554C>A	NCBI36