Canonical Allele Identifier: CA769945315
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1331091991
gnomAD v3: 2-51936048-GTATA-G
gnomAD v4: 2-51936048-GTATA-G
MyVariant Identifiers: chr2:g.52163187_52163190del (hg19) chr2:g.51936049_51936052del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936058_51936061del , CM000664.2:g.51936058_51936061del GRCh38
NC_000002.11:g.52163196_52163199del , CM000664.1:g.52163196_52163199del GRCh37
NC_000002.10:g.52016700_52016703del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74570_879+74573del
NR_135237.1:n.879+74570_879+74573del
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