Canonical Allele Identifier: CA48266089
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs70958692
gnomAD v2: 2-52163214-G-GTA
gnomAD v3: 2-51936076-G-GTA
gnomAD v4: 2-51936076-G-GTA
MyVariant Identifiers: chr2:g.52163227_52163228insAT (hg19) chr2:g.52163216_52163217insTA (hg19) chr2:g.52163214_52163215insTA (hg19) chr2:g.51936089_51936090insAT (hg38) chr2:g.51936078_51936079insTA (hg38) chr2:g.51936076_51936077insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936088_51936089dup , CM000664.2:g.51936088_51936089dup GRCh38
NC_000002.11:g.52163226_52163227dup , CM000664.1:g.52163226_52163227dup GRCh37
NC_000002.10:g.52016730_52016731dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74600_879+74601dup
NR_135237.1:n.879+74600_879+74601dup
Search 100 bp 5'
Search 100 bp 3'