Canonical Allele Identifier: CA10581226

Gene:

Linked Data

• ClinVar Variation Id: 235098
• ClinVar RCV Id: RCV000223874
• dbSNP Id: rs876661321
• MyVariant Identifiers: chr3:g.186559503G>T (hg19) ; chr3:g.186841714G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186841714G>T , CM000665.2:g.186841714G>T	GRCh38
NC_000003.11:g.186559503G>T , CM000665.1:g.186559503G>T	GRCh37
NC_000003.10:g.188042197G>T	NCBI36
NG_021140.1:g.4041G>T