Canonical Allele Identifier: CA658653869
Gene:

Linked Data

ClinVar Variation Id: 444076
ClinVar RCV Id: RCV000513227

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30307936_30311263del , CM000685.2:g.30307936_30311263del GRCh38
NC_000023.10:g.30326053_30329380del , CM000685.1:g.30326053_30329380del GRCh37
NC_000023.9:g.30235974_30239301del NCBI36
NG_009814.1:g.3116_6443del