Canonical Allele Identifier: CA271505107
Gene:

Linked Data

ClinVar Variation Id: 1221122
ClinVar RCV Id: RCV001595684
dbSNP Id: rs58967026
gnomAD v2: 15-65322166-C-CTTTATTTATTTATTTA
gnomAD v3: 15-65029828-C-CTTTATTTATTTATTTA
gnomAD v4: 15-65029828-C-CTTTATTTATTTATTTA
MyVariant Identifiers: chr15:g.65322170_65322171insTTTATTTATTTATTTA (hg19) chr15:g.65322166_65322167insTTTATTTATTTATTTA (hg19) chr15:g.65029832_65029833insTTTATTTATTTATTTA (hg38) chr15:g.65029828_65029829insTTTATTTATTTATTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029848_65029863dup , CM000677.2:g.65029848_65029863dup GRCh38
NC_000015.9:g.65322186_65322201dup , CM000677.1:g.65322186_65322201dup GRCh37
NC_000015.8:g.63109239_63109254dup NCBI36
NG_029184.1:g.4796_4811dup
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