Canonical Allele Identifier: CA915942476
Gene:

Linked Data

ClinVar Variation Id: 692082
ClinVar RCV Id: RCV000853385
dbSNP Id: rs1575295176

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467718_48467735del , CM000665.2:g.48467718_48467735del GRCh38
NC_000003.11:g.48509117_48509134del , CM000665.1:g.48509117_48509134del GRCh37
NC_000003.10:g.48484121_48484138del NCBI36
NG_009820.1:g.6889_6906del
NG_033100.1:g.38126_38143del
NG_009820.2:g.6889_6906del