Canonical Allele Identifier: CA185710860

Gene:

Linked Data

• ClinVar Variation Id: 979040
• ClinVar RCV Id: RCV001257963
• dbSNP Id: rs188140481
• gnomAD v2: 8-128191672-T-A
• gnomAD v3: 8-127179427-T-A
• gnomAD v4: 8-127179427-T-A
• MyVariant Identifiers: chr8:g.128191672T>A (hg19) ; chr8:g.127179427T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127179427T>A , CM000670.2:g.127179427T>A	GRCh38
NC_000008.10:g.128191672T>A , CM000670.1:g.128191672T>A	GRCh37
NC_000008.9:g.128260854T>A	NCBI36