Canonical Allele Identifier: CA16329102

Gene:

Linked Data

• ClinVar Variation Id: 1181642
• ClinVar RCV Id: RCV001539082
• dbSNP Id: rs9644636
• gnomAD v2: 8-19824896-T-G
• gnomAD v3: 8-19967385-T-G
• gnomAD v4: 8-19967385-T-G
• MyVariant Identifiers: chr8:g.19824896T>G (hg19) ; chr8:g.19967385T>G (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19967385T>G , CM000670.2:g.19967385T>G	GRCh38
NC_000008.10:g.19824896T>G , CM000670.1:g.19824896T>G	GRCh37
NC_000008.9:g.19869176T>G	NCBI36
NG_008855.1:g.33315T>G
NG_008855.2:g.70669T>G