Canonical Allele Identifier: CA14082374

Gene:

Linked Data

• ClinVar Variation Id: 1233353
• ClinVar RCV Id: RCV001617478
• dbSNP Id: rs514049
• gnomAD v2: 15-59042363-C-A
• gnomAD v3: 15-58750164-C-A
• gnomAD v4: 15-58750164-C-A
• MyVariant Identifiers: chr15:g.59042363C>A (hg19) ; chr15:g.58750164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58750164C>A , CM000677.2:g.58750164C>A	GRCh38
NC_000015.9:g.59042363C>A , CM000677.1:g.59042363C>A	GRCh37
NC_000015.8:g.56829655C>A	NCBI36
NG_033876.1:g.4815G>T
NG_033876.2:g.4544G>T