Canonical Allele Identifier: CA1250396851
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935740T= , CM000664.2:g.51935740T= GRCh38
NC_000002.11:g.52162878T= , CM000664.1:g.52162878T= GRCh37
NC_000002.10:g.52016382T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74252T=
NR_135237.1:n.879+74252T=