Canonical Allele Identifier: CA532709293
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1491318624
gnomAD v2: 2-52163199-T-TATATATATATATGTATATATATATAC
gnomAD v3: 2-51936061-T-TATATATATATATGTATATATATATAC
gnomAD v4: 2-51936061-T-TATATATATATATGTATATATATATAC
MyVariant Identifiers: chr2:g.52163199_52163200insATATATATATATGTATATATATATAC (hg19) chr2:g.51936061_51936062insATATATATATATGTATATATATATAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936061_51936062insATATATATATATGTATATATATATAC , CM000664.2:g.51936061_51936062insATATATATATATGTATATATATATAC GRCh38
NC_000002.11:g.52163199_52163200insATATATATATATGTATATATATATAC , CM000664.1:g.52163199_52163200insATATATATATATGTATATATATATAC GRCh37
NC_000002.10:g.52016703_52016704insATATATATATATGTATATATATATAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74573_879+74574insATATATATATATGTATATATATATAC
NR_135237.1:n.879+74573_879+74574insATATATATATATGTATATATATATAC
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