Canonical Allele Identifier: CA2699128061
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667844204

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935854G>T , CM000664.2:g.51935854G>T GRCh38
NC_000002.11:g.52162992G>T , CM000664.1:g.52162992G>T GRCh37
NC_000002.10:g.52016496G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74366G>T
NR_135237.1:n.879+74366G>T