Canonical Allele Identifier: CA1250396892
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935788G= , CM000664.2:g.51935788G= GRCh38
NC_000002.11:g.52162926G= , CM000664.1:g.52162926G= GRCh37
NC_000002.10:g.52016430G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74300G=
NR_135237.1:n.879+74300G=