Canonical Allele Identifier: CA15303895

Gene:

Linked Data

• ClinVar Variation Id: 444126
• ClinVar RCV Id: RCV000626362
• dbSNP Id: rs2788865
• gnomAD v2: 4-26446006-G-A
• gnomAD v3: 4-26444384-G-A
• gnomAD v4: 4-26444384-G-A
• MyVariant Identifiers: chr4:g.26446006G>A (hg19) ; chr4:g.26444384G>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26444384G>A , CM000666.2:g.26444384G>A	GRCh38
NC_000004.11:g.26446006G>A , CM000666.1:g.26446006G>A	GRCh37
NC_000004.10:g.26055104G>A	NCBI36