Canonical Allele Identifier: CA14471957

Gene:

Linked Data

• ClinVar Variation Id: 1229047
• ClinVar RCV Id: RCV001609287
• dbSNP Id: rs113819303
• gnomAD v2: 17-1303788-C-A
• gnomAD v3: 17-1400494-C-A
• gnomAD v4: 17-1400494-C-A
• MyVariant Identifiers: chr17:g.1303788C>A (hg19) ; chr17:g.1400494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1400494C>A , CM000679.2:g.1400494C>A	GRCh38
NC_000017.10:g.1303788C>A , CM000679.1:g.1303788C>A	GRCh37
NC_000017.9:g.1250538C>A	NCBI36
NG_009233.1:g.4769G>T