Canonical Allele Identifier: CA343751
Gene:

Linked Data

ClinVar Variation Id: 39279
ClinVar RCV Id: RCV000032557
dbSNP Id: rs199422255

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765301_169765302del , CM000665.2:g.169765301_169765302del GRCh38
NC_000003.11:g.169483089_169483090del , CM000665.1:g.169483089_169483090del GRCh37
NC_000003.10:g.170965783_170965784del NCBI36
NG_016363.1:g.4761_4762del , LRG_347:g.4761_4762del