Canonical Allele Identifier: CA527264269
Gene:

Linked Data

ClinVar Variation Id: 1255258
ClinVar RCV Id: RCV001653367
dbSNP Id: rs1553255689
gnomAD v2: 1-171622064-T-TATACACACACAC
gnomAD v3: 1-171652924-T-TATACACACACAC
gnomAD v4: 1-171652924-T-TATACACACACAC
MyVariant Identifiers: chr1:g.171622066delinsTACACACACACAC (hg19) chr1:g.171622064_171622065insATACACACACAC (hg19) chr1:g.171652926delinsTACACACACACAC (hg38) chr1:g.171652924_171652925insATACACACACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652925_171652926insTACACACACACA , CM000663.2:g.171652925_171652926insTACACACACACA GRCh38
NC_000001.10:g.171622065_171622066insTACACACACACA , CM000663.1:g.171622065_171622066insTACACACACACA GRCh37
NC_000001.9:g.169888688_169888689insTACACACACACA NCBI36
NG_008859.1:g.4709_4710insGTGTGTGTGTAT
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