Canonical Allele Identifier: CA356578
Gene:

Linked Data

ClinVar Variation Id: 242644
ClinVar RCV Id: RCV000114378
PubMed: PMID:16540753 PMID:17079880 PMID:20301691
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.[34645666_34648827del;34648944_34651238delinsGAATAGACCCCA] , CM000671.2:g.[34645666_34648827del;34648944_34651238delinsGAATAGACCCCA] GRCh38
NC_000009.11:g.[34645663_34648824del;34648941_34651235delinsGAATAGACCCCA] , CM000671.1:g.[34645663_34648824del;34648941_34651235delinsGAATAGACCCCA] GRCh37
NC_000009.10:g.[34635663_34638824del;34638941_34641235delinsGAATAGACCCCA] NCBI36
NG_009029.2:g.[4078_7239del;7356_9650delinsGAATAGACCCCA]
Search 100 bp 5'
Search 100 bp 3'