Canonical Allele Identifier: CA2499219886

Gene:

Linked Data

• ClinVar Variation Id: 1066356
• ClinVar RCV Id: RCV001377331
• dbSNP Id: rs2131809458

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658019_35658041dup , CM000671.2:g.35658019_35658041dup	GRCh38
NC_000009.11:g.35658016_35658038dup , CM000671.1:g.35658016_35658038dup	GRCh37
NC_000009.10:g.35648016_35648038dup	NCBI36
NG_017041.1:g.4978_5000dup , LRG_163:g.4978_5000dup
NG_033120.1:g.4730_4752dup