Canonical Allele Identifier: CA304067560

Gene:

Linked Data

• ClinVar Variation Id: 1222029
• ClinVar RCV Id: RCV001595847
• dbSNP Id: rs188279623
• gnomAD v2: 19-1401679-C-T
• gnomAD v3: 19-1401680-C-T
• gnomAD v4: 19-1401680-C-T
• MyVariant Identifiers: chr19:g.1401679C>T (hg19) ; chr19:g.1401680C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1401680C>T , CM000681.2:g.1401680C>T	GRCh38
NC_000019.9:g.1401679C>T , CM000681.1:g.1401679C>T	GRCh37
NC_000019.8:g.1352679C>T	NCBI36
NG_009785.1:g.4874G>A