Canonical Allele Identifier: CA192745792

Gene:

Linked Data

• ClinVar Variation Id: 658456
• ClinVar RCV Id: RCV001507749 ; RCV000815283
• dbSNP Id: rs551474332
• gnomAD v2: 9-35658068-T-C
• gnomAD v3: 9-35658071-T-C
• gnomAD v4: 9-35658071-T-C
• MyVariant Identifiers: chr9:g.35658068T>C (hg19) ; chr9:g.35658071T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658071T>C , CM000671.2:g.35658071T>C	GRCh38
NC_000009.11:g.35658068T>C , CM000671.1:g.35658068T>C	GRCh37
NC_000009.10:g.35648068T>C	NCBI36
NG_017041.1:g.4948A>G , LRG_163:g.4948A>G
NG_033120.1:g.4782T>C