Canonical Allele Identifier: CA1250280001
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732020A= , CM000664.2:g.51732020A= GRCh38
NC_000002.11:g.51959158A= , CM000664.1:g.51959158A= GRCh37
NC_000002.10:g.51812662A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30069A=
NR_135237.1:n.754-30069A=