Canonical Allele Identifier: CA212291
Gene:

Linked Data

ClinVar Variation Id: 157197
ClinVar RCV Id: RCV000161623
MyVariant Identifiers: chr11:g.18949220_18956690del (hg19) chr11:g.18927673_18935143del (hg38)
PubMed: PMID:25666259
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18927673_18935143del , CM000673.2:g.18927673_18935143del GRCh38
NC_000011.9:g.18949220_18956690del , CM000673.1:g.18949220_18956690del GRCh37
NC_000011.8:g.18905796_18913266del NCBI36
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