Canonical Allele Identifier: CA2696853

Gene:

Linked Data

• ClinVar Variation Id: 242267
• ClinVar RCV Id: RCV001561876 ; RCV001820784
• dbSNP Id: rs540289812
• ExAC: 3:169482947 G / C
• gnomAD v2: 3-169482947-G-C
• gnomAD v3: 3-169765159-G-C
• gnomAD v4: 3-169765159-G-C
• MyVariant Identifiers: chr3:g.169482947G>C (hg19) ; chr3:g.169765159G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765159G>C , CM000665.2:g.169765159G>C	GRCh38
NC_000003.11:g.169482947G>C , CM000665.1:g.169482947G>C	GRCh37
NC_000003.10:g.170965641G>C	NCBI36
NG_016363.1:g.4902C>G , LRG_347:g.4902C>G