Canonical Allele Identifier: CA11427621

Gene:

Linked Data

• ClinVar Variation Id: 440330
• ClinVar RCV Id: RCV000508369
• dbSNP Id: rs2293607
• gnomAD v2: 3-169482335-T-C
• gnomAD v3: 3-169764547-T-C
• gnomAD v4: 3-169764547-T-C
• MyVariant Identifiers: chr3:g.169482335T>C (hg19) ; chr3:g.169764547T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764547T>C , CM000665.2:g.169764547T>C	GRCh38
NC_000003.11:g.169482335T>C , CM000665.1:g.169482335T>C	GRCh37
NC_000003.10:g.170965029T>C	NCBI36
NG_016363.1:g.5514A>G , LRG_347:g.5514A>G