Canonical Allele Identifier: CA1139660923

Gene:

Linked Data

• ClinVar Variation Id: 965369
• ClinVar RCV Id: RCV001239803 ; RCV002051924
• dbSNP Id: rs1554651349

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658015_35658041dup , CM000671.2:g.35658015_35658041dup	GRCh38
NC_000009.11:g.35658012_35658038dup , CM000671.1:g.35658012_35658038dup	GRCh37
NC_000009.10:g.35648012_35648038dup	NCBI36
NG_017041.1:g.4979_5005dup , LRG_163:g.4979_5005dup
NG_033120.1:g.4726_4752dup