Canonical Allele Identifier: CA5045900

Gene:

Linked Data

• ClinVar Variation Id: 2414256
• ClinVar RCV Id: RCV003106589
• dbSNP Id: rs768701060
• ExAC: 9:35658064 G / A
• gnomAD v2: 9-35658064-G-A
• gnomAD v3: 9-35658067-G-A
• gnomAD v4: 9-35658067-G-A
• MyVariant Identifiers: chr9:g.35658064G>A (hg19) ; chr9:g.35658064_35658065delinsAT (hg19) ; chr9:g.35658067G>A (hg38) ; chr9:g.35658067_35658068delinsAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658067G>A , CM000671.2:g.35658067G>A	GRCh38
NC_000009.11:g.35658064G>A , CM000671.1:g.35658064G>A	GRCh37
NC_000009.10:g.35648064G>A	NCBI36
NG_017041.1:g.4952C>T , LRG_163:g.4952C>T
NG_033120.1:g.4778G>A