Canonical Allele Identifier: CA915947439

Gene:

Linked Data

• ClinVar Variation Id: 660541
• ClinVar RCV Id: RCV000817755
• dbSNP Id: rs1587919053
• gnomAD v4: 9-35658016-A-ACCACGTCCTCAGCTTCACAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658017_35658038dup , CM000671.2:g.35658017_35658038dup	GRCh38
NC_000009.11:g.35658014_35658035dup , CM000671.1:g.35658014_35658035dup	GRCh37
NC_000009.10:g.35648014_35648035dup	NCBI36
NG_017041.1:g.4981_5002dup , LRG_163:g.4981_5002dup
NG_033120.1:g.4728_4749dup