Canonical Allele Identifier: CA87625118

Gene:

Linked Data

• ClinVar Variation Id: 1186345
• ClinVar RCV Id: RCV001545411 ; RCV001821874 ; RCV003940990
• dbSNP Id: rs116780570
• gnomAD v2: 3-169483093-C-T
• gnomAD v3: 3-169765305-C-T
• gnomAD v4: 3-169765305-C-T
• MyVariant Identifiers: chr3:g.169483093C>T (hg19) ; chr3:g.169765305C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765305C>T , CM000665.2:g.169765305C>T	GRCh38
NC_000003.11:g.169483093C>T , CM000665.1:g.169483093C>T	GRCh37
NC_000003.10:g.170965787C>T	NCBI36
NG_016363.1:g.4756G>A , LRG_347:g.4756G>A