Canonical Allele Identifier: CA490827055
Gene:

Linked Data

ClinVar Variation Id: 1179583
ClinVar RCV Id: RCV001536600
dbSNP Id: rs764189876
gnomAD v2: 15-65322165-G-GATTTATTTATTT
gnomAD v3: 15-65029827-G-GATTTATTTATTT
gnomAD v4: 15-65029827-G-GATTTATTTATTT
MyVariant Identifiers: chr15:g.65322165_65322166insATTTATTTATTT (hg19) chr15:g.65029827_65029828insATTTATTTATTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029827_65029828insATTTATTTATTT , CM000677.2:g.65029827_65029828insATTTATTTATTT GRCh38
NC_000015.9:g.65322165_65322166insATTTATTTATTT , CM000677.1:g.65322165_65322166insATTTATTTATTT GRCh37
NC_000015.8:g.63109218_63109219insATTTATTTATTT NCBI36
NG_029184.1:g.4812_4813insAAATAAATAAAT
Search 100 bp 5'
Search 100 bp 3'