Canonical Allele Identifier: CA587570260

Gene:

Linked Data

• ClinVar Variation Id: 856051
• ClinVar RCV Id: RCV001061436 ; RCV001827389 ; RCV002479362
• dbSNP Id: rs1479868789
• gnomAD v2: 9-35658041-T-C
• gnomAD v3: 9-35658044-T-C
• gnomAD v4: 9-35658044-T-C
• MyVariant Identifiers: chr9:g.35658041T>C (hg19) ; chr9:g.35658044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658044T>C , CM000671.2:g.35658044T>C	GRCh38
NC_000009.11:g.35658041T>C , CM000671.1:g.35658041T>C	GRCh37
NC_000009.10:g.35648041T>C	NCBI36
NG_017041.1:g.4975A>G , LRG_163:g.4975A>G
NG_033120.1:g.4755T>C