Canonical Allele Identifier: CA769944719
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1163649006
gnomAD v3: 2-51935998-ATATATATG-A
gnomAD v4: 2-51935998-ATATATATG-A
MyVariant Identifiers: chr2:g.52163137_52163144del (hg19) chr2:g.51935999_51936006del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936006_51936013del , CM000664.2:g.51936006_51936013del GRCh38
NC_000002.11:g.52163144_52163151del , CM000664.1:g.52163144_52163151del GRCh37
NC_000002.10:g.52016648_52016655del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74518_879+74525del
NR_135237.1:n.879+74518_879+74525del
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