Canonical Allele Identifier: CA918446897
Gene:

Linked Data

ClinVar Variation Id: 1066913
ClinVar RCV Id: RCV001378039
dbSNP Id: rs1218494857
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658022_35658023insTCTCAGCTTCACAGAGACGT , CM000671.2:g.35658022_35658023insTCTCAGCTTCACAGAGACGT GRCh38
NC_000009.11:g.35658019_35658020insTCTCAGCTTCACAGAGACGT , CM000671.1:g.35658019_35658020insTCTCAGCTTCACAGAGACGT GRCh37
NC_000009.10:g.35648019_35648020insTCTCAGCTTCACAGAGACGT NCBI36
NG_017041.1:g.5000_5001insCTCTGTGAAGCTGAGAACGT , LRG_163:g.5000_5001insCTCTGTGAAGCTGAGAACGT
NG_033120.1:g.4733_4734insTCTCAGCTTCACAGAGACGT
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