Canonical Allele Identifier: CA2622977048

Gene:

Linked Data

• ClinVar Variation Id: 2878977
• ClinVar RCV Id: RCV003626476
• gnomAD v4: 13-48303712-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303712G>T , CM000675.2:g.48303712G>T	GRCh38
NC_000013.10:g.48877848G>T , CM000675.1:g.48877848G>T	GRCh37
NC_000013.9:g.47775849G>T	NCBI36
NG_009009.1:g.4966G>T , LRG_517:g.4966G>T