Canonical Allele Identifier: CA176095635

Gene:

Linked Data

• ClinVar Variation Id: 674251
• ClinVar RCV Id: RCV000833565
• dbSNP Id: rs149596192
• gnomAD v2: 8-42995466-G-A
• gnomAD v3: 8-43140323-G-A
• gnomAD v4: 8-43140323-G-A
• MyVariant Identifiers: chr8:g.42995466G>A (hg19) ; chr8:g.43140323G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140323G>A , CM000670.2:g.43140323G>A	GRCh38
NC_000008.10:g.42995466G>A , CM000670.1:g.42995466G>A	GRCh37
NC_000008.9:g.43114623G>A	NCBI36
NG_009552.1:g.4875G>A