Canonical Allele Identifier: CA490827057
Gene:

Linked Data

ClinVar Variation Id: 1239198
ClinVar RCV Id: RCV001636106
dbSNP Id: rs58967026
gnomAD v2: 15-65322166-C-CTTTATTTATTTATTTATTTA
gnomAD v3: 15-65029828-C-CTTTATTTATTTATTTATTTA
gnomAD v4: 15-65029828-C-CTTTATTTATTTATTTATTTA
MyVariant Identifiers: chr15:g.65322170_65322171insTTTATTTATTTATTTATTTA (hg19) chr15:g.65322166_65322167insTTTATTTATTTATTTATTTA (hg19) chr15:g.65029832_65029833insTTTATTTATTTATTTATTTA (hg38) chr15:g.65029828_65029829insTTTATTTATTTATTTATTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029844_65029863dup , CM000677.2:g.65029844_65029863dup GRCh38
NC_000015.9:g.65322182_65322201dup , CM000677.1:g.65322182_65322201dup GRCh37
NC_000015.8:g.63109235_63109254dup NCBI36
NG_029184.1:g.4792_4811dup
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