Canonical Allele Identifier: CA769945207
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1491265288
gnomAD v3: 2-51936033-CGT-C
gnomAD v4: 2-51936033-CGT-C
MyVariant Identifiers: chr2:g.52163172_52163173del (hg19) chr2:g.51936034_51936035del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936034_51936035del , CM000664.2:g.51936034_51936035del GRCh38
NC_000002.11:g.52163172_52163173del , CM000664.1:g.52163172_52163173del GRCh37
NC_000002.10:g.52016676_52016677del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74546_879+74547del
NR_135237.1:n.879+74546_879+74547del
Search 100 bp 5'
Search 100 bp 3'