Canonical Allele Identifier: CA587570267

Gene:

Linked Data

• ClinVar Variation Id: 1943921
• ClinVar RCV Id: RCV002670979
• dbSNP Id: rs775290179
• gnomAD v2: 9-35658049-C-T
• gnomAD v4: 9-35658052-C-T
• MyVariant Identifiers: chr9:g.35658049C>T (hg19) ; chr9:g.35658052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658052C>T , CM000671.2:g.35658052C>T	GRCh38
NC_000009.11:g.35658049C>T , CM000671.1:g.35658049C>T	GRCh37
NC_000009.10:g.35648049C>T	NCBI36
NG_017041.1:g.4967G>A , LRG_163:g.4967G>A
NG_033120.1:g.4763C>T