Canonical Allele Identifier: CA490827054
Gene:

Linked Data

ClinVar Variation Id: 1260854
ClinVar RCV Id: RCV001669671
dbSNP Id: rs764189876
gnomAD v2: 15-65322165-G-GATTTATTTATTTATTTATTT
gnomAD v3: 15-65029827-G-GATTTATTTATTTATTTATTT
gnomAD v4: 15-65029827-G-GATTTATTTATTTATTTATTT
MyVariant Identifiers: chr15:g.65322165_65322166insATTTATTTATTTATTTATTT (hg19) chr15:g.65029827_65029828insATTTATTTATTTATTTATTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029827_65029828insATTTATTTATTTATTTATTT , CM000677.2:g.65029827_65029828insATTTATTTATTTATTTATTT GRCh38
NC_000015.9:g.65322165_65322166insATTTATTTATTTATTTATTT , CM000677.1:g.65322165_65322166insATTTATTTATTTATTTATTT GRCh37
NC_000015.8:g.63109218_63109219insATTTATTTATTTATTTATTT NCBI36
NG_029184.1:g.4812_4813insAAATAAATAAATAAATAAAT
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