Canonical Allele Identifier: CA14423806

Gene:

Linked Data

• ClinVar Variation Id: 1231511
• ClinVar RCV Id: RCV001610167
• dbSNP Id: rs4291
• gnomAD v2: 17-61554194-T-A
• gnomAD v3: 17-63476833-T-A
• gnomAD v4: 17-63476833-T-A
• MyVariant Identifiers: chr17:g.61554194T>A (hg19) ; chr17:g.63476833T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63476833T>A , CM000679.2:g.63476833T>A	GRCh38
NC_000017.10:g.61554194T>A , CM000679.1:g.61554194T>A	GRCh37
NC_000017.9:g.58907926T>A	NCBI36
NG_011648.1:g.4761T>A