Canonical Allele Identifier: CA11915807

Gene:

Linked Data

• ClinVar Variation Id: 375479
• ClinVar RCV Id: RCV000498732 ; RCV001787099
• dbSNP Id: rs2735940
• gnomAD v2: 5-1296486-A-G
• gnomAD v3: 5-1296371-A-G
• gnomAD v4: 5-1296371-A-G
• MyVariant Identifiers: chr5:g.1296486A>G (hg19) ; chr5:g.1296371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1296371A>G , CM000667.2:g.1296371A>G	GRCh38
NC_000005.9:g.1296486A>G , CM000667.1:g.1296486A>G	GRCh37
NC_000005.8:g.1349486A>G	NCBI36
NG_009265.1:g.3677T>C , LRG_343:g.3677T>C