Canonical Allele Identifier: CA124670
Gene:

Linked Data

ClinVar Variation Id: 15061
ClinVar RCV Id: RCV000016208 RCV000415449 RCV001196231
MyVariant Identifiers: chr11:g.5247800_5255214del (hg19) chr11:g.5226570_5233984del (hg38)
PubMed: PMID:1347969 PMID:1693293 PMID:2442092 PMID:4625560 PMID:5660684 PMID:5964983 PMID:13892631 PMID:14133899
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226570_5233984del , CM000673.2:g.5226570_5233984del GRCh38
NC_000011.9:g.5247800_5255214del , CM000673.1:g.5247800_5255214del GRCh37
NC_000011.8:g.5204376_5211790del NCBI36
NG_000007.3:g.63632_71046del
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