Canonical Allele Identifier: CA2499219888
Gene:

Linked Data

ClinVar Variation Id: 1066656
ClinVar RCV Id: RCV001377707
dbSNP Id: rs2131809584
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658064_35658065insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT , CM000671.2:g.35658064_35658065insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT GRCh38
NC_000009.11:g.35658061_35658062insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT , CM000671.1:g.35658061_35658062insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT GRCh37
NC_000009.10:g.35648061_35648062insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT NCBI36
NG_017041.1:g.4998_4999insCCTAACCATAAAACAAAATTTCTTTAGGGCTATAAAATACTACTCTGTGAAGCTGAGGAC , LRG_163:g.4998_4999insCCTAACCATAAAACAAAATTTCTTTAGGGCTATAAAATACTACTCTGTGAAGCTGAGGAC
NG_033120.1:g.4775_4776insTTGTTTTATGGTTAGGGTCCTCAGCTTCACAGAGTAGTATTTTATAGCCCTAAAGAAATT
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