Canonical Allele Identifier: CA1250396883
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935769G= , CM000664.2:g.51935769G= GRCh38
NC_000002.11:g.52162907G= , CM000664.1:g.52162907G= GRCh37
NC_000002.10:g.52016411G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74281G=
NR_135237.1:n.879+74281G=