Canonical Allele Identifier: CA2739269246
Gene:

Linked Data

ClinVar Variation Id: 2831884
ClinVar RCV Id: RCV003758286
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658064_35658065insTTGTTTATAGCCCTAAAGAAATT , CM000671.2:g.35658064_35658065insTTGTTTATAGCCCTAAAGAAATT GRCh38
NC_000009.11:g.35658061_35658062insTTGTTTATAGCCCTAAAGAAATT , CM000671.1:g.35658061_35658062insTTGTTTATAGCCCTAAAGAAATT GRCh37
NC_000009.10:g.35648061_35648062insTTGTTTATAGCCCTAAAGAAATT NCBI36
NG_017041.1:g.4974_4975insCAAAATTTCTTTAGGGCTATAAA , LRG_163:g.4974_4975insCAAAATTTCTTTAGGGCTATAAA
NG_033120.1:g.4775_4776insTTGTTTATAGCCCTAAAGAAATT
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