Canonical Allele Identifier: CA249842000

Gene:

Linked Data

• ClinVar Variation Id: 2912983
• ClinVar RCV Id: RCV003627463
• dbSNP Id: rs768638029
• gnomAD v3: 13-48303742-G-A
• gnomAD v4: 13-48303742-G-A
• MyVariant Identifiers: chr13:g.48877878G>A (hg19) ; chr13:g.48303742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303742G>A , CM000675.2:g.48303742G>A	GRCh38
NC_000013.10:g.48877878G>A , CM000675.1:g.48877878G>A	GRCh37
NC_000013.9:g.47775879G>A	NCBI36
NG_009009.1:g.4996G>A , LRG_517:g.4996G>A