Canonical Allele Identifier: CA2622977082

Gene:

Linked Data

• ClinVar Variation Id: 3013144
• ClinVar RCV Id: RCV003870239
• gnomAD v4: 13-48303741-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303741C>T , CM000675.2:g.48303741C>T	GRCh38
NC_000013.10:g.48877877C>T , CM000675.1:g.48877877C>T	GRCh37
NC_000013.9:g.47775878C>T	NCBI36
NG_009009.1:g.4995C>T , LRG_517:g.4995C>T