Canonical Allele Identifier: CA1139660924

Gene:

Linked Data

• ClinVar Variation Id: 968652
• ClinVar RCV Id: RCV001243838
• dbSNP Id: rs1823629969

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658016_35658035dup , CM000671.2:g.35658016_35658035dup	GRCh38
NC_000009.11:g.35658013_35658032dup , CM000671.1:g.35658013_35658032dup	GRCh37
NC_000009.10:g.35648013_35648032dup	NCBI36
NG_017041.1:g.4985_5004dup , LRG_163:g.4985_5004dup
NG_033120.1:g.4727_4746dup