Canonical Allele Identifier: CA192745748

Gene:

Linked Data

• ClinVar Variation Id: 516512
• ClinVar RCV Id: RCV000610071 ; RCV000672983 ; RCV001239736
• dbSNP Id: rs555890962
• gnomAD v2: 9-35658019-T-C
• gnomAD v3: 9-35658022-T-C
• gnomAD v4: 9-35658022-T-C
• MyVariant Identifiers: chr9:g.35658019T>C (hg19) ; chr9:g.35658022T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658022T>C , CM000671.2:g.35658022T>C	GRCh38
NC_000009.11:g.35658019T>C , CM000671.1:g.35658019T>C	GRCh37
NC_000009.10:g.35648019T>C	NCBI36
NG_017041.1:g.4997A>G , LRG_163:g.4997A>G
NG_033120.1:g.4733T>C