Canonical Allele Identifier: CA315526002

Gene:

Linked Data

• ClinVar Variation Id: 444108
• ClinVar RCV Id: RCV000626344
• dbSNP Id: rs143311170
• gnomAD v2: 20-43785791-A-G
• gnomAD v3: 20-45157150-A-G
• gnomAD v4: 20-45157150-A-G
• MyVariant Identifiers: chr20:g.43785791A>G (hg19) ; chr20:g.45157150A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45157150A>G , CM000682.2:g.45157150A>G	GRCh38
NC_000020.10:g.43785791A>G , CM000682.1:g.43785791A>G	GRCh37
NC_000020.9:g.43219205A>G	NCBI36