Canonical Allele Identifier: CA192745793

Gene:

Linked Data

• ClinVar Variation Id: 1024314
• ClinVar RCV Id: RCV001324480
• dbSNP Id: rs181777676
• gnomAD v3: 9-35658072-A-G
• gnomAD v4: 9-35658072-A-G
• MyVariant Identifiers: chr9:g.35658069A>G (hg19) ; chr9:g.35658072A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658072A>G , CM000671.2:g.35658072A>G	GRCh38
NC_000009.11:g.35658069A>G , CM000671.1:g.35658069A>G	GRCh37
NC_000009.10:g.35648069A>G	NCBI36
NG_017041.1:g.4947T>C , LRG_163:g.4947T>C
NG_033120.1:g.4783A>G