Canonical Allele Identifier: CA341387
Gene:

Linked Data

ClinVar Variation Id: 16166
ClinVar RCV Id: RCV000017549
MyVariant Identifiers: chr2:g.27532179_27533753delinsCAGGC (hg19) chr2:g.27309311_27310885delinsCAGGC (hg38)
PubMed: PMID:18695062 PMID:22593919
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27309311_27310884delinsCAGG , CM000664.2:g.27309311_27310884delinsCAGG GRCh38
NC_000002.11:g.27532179_27533752delinsCAGG , CM000664.1:g.27532179_27533752delinsCAGG GRCh37
NC_000002.10:g.27385683_27387256delinsCAGG NCBI36
NG_008075.1:g.16680_18253delinsCCTG
NG_033055.1:g.2379_3952delinsCCTG
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