Canonical Allele Identifier: CA330635
Gene:

Linked Data

ClinVar Variation Id: 89592
ClinVar RCV Id: RCV000075061

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993167_36997315del , CM000665.2:g.36993167_36997315del GRCh38
NC_000003.11:g.37034658_37038806del , CM000665.1:g.37034658_37038806del GRCh37
NC_000003.10:g.37009662_37013810del NCBI36
NG_007109.2:g.4818_8966del , LRG_216:g.4818_8966del
NG_008418.1:g.993_5141del