Canonical Allele Identifier: CA1139660926

Gene:

Linked Data

• ClinVar Variation Id: 918169
• ClinVar RCV Id: RCV001175611 ; RCV001377210
• dbSNP Id: rs1823634410
• gnomAD v4: 9-35658020-C-CGTCCTCAGCTTCACA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658022_35658036dup , CM000671.2:g.35658022_35658036dup	GRCh38
NC_000009.11:g.35658019_35658033dup , CM000671.1:g.35658019_35658033dup	GRCh37
NC_000009.10:g.35648019_35648033dup	NCBI36
NG_017041.1:g.4984_4998dup , LRG_163:g.4984_4998dup
NG_033120.1:g.4733_4747dup