Canonical Allele Identifier: CA532709159
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1244465437
gnomAD v2: 2-52163133-CATATATATATGTATATATATATATGT-C
gnomAD v3: 2-51935995-CATATATATATGTATATATATATATGT-C
gnomAD v4: 2-51935995-CATATATATATGTATATATATATATGT-C
MyVariant Identifiers: chr2:g.52163134_52163159del (hg19) chr2:g.52163144_52163189delinsACGTATATATATATATGTAT (hg19) chr2:g.51935996_51936021del (hg38) chr2:g.51936006_51936051delinsACGTATATATATATATGTAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936006_51936031del , CM000664.2:g.51936006_51936031del GRCh38
NC_000002.11:g.52163144_52163169del , CM000664.1:g.52163144_52163169del GRCh37
NC_000002.10:g.52016648_52016673del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74518_879+74543del
NR_135237.1:n.879+74518_879+74543del
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