Canonical Allele Identifier: CA14423808

Gene:

Linked Data

• ClinVar Variation Id: 1285756
• ClinVar RCV Id: RCV001708050
• dbSNP Id: rs4292
• gnomAD v2: 17-61554341-C-T
• gnomAD v3: 17-63476980-C-T
• gnomAD v4: 17-63476980-C-T
• MyVariant Identifiers: chr17:g.61554341C>T (hg19) ; chr17:g.63476980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63476980C>T , CM000679.2:g.63476980C>T	GRCh38
NC_000017.10:g.61554341C>T , CM000679.1:g.61554341C>T	GRCh37
NC_000017.9:g.58908073C>T	NCBI36
NG_011648.1:g.4908C>T