Canonical Allele Identifier: CA1250397372
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667850912

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936011_51936012insGTAT , CM000664.2:g.51936011_51936012insGTAT GRCh38
NC_000002.11:g.52163149_52163150insGTAT , CM000664.1:g.52163149_52163150insGTAT GRCh37
NC_000002.10:g.52016653_52016654insGTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74523_879+74524insGTAT
NR_135237.1:n.879+74523_879+74524insGTAT