Canonical Allele Identifier: CA1250108722
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440617C= , CM000664.2:g.51440617C= GRCh38
NC_000002.11:g.51667755C= , CM000664.1:g.51667755C= GRCh37
NC_000002.10:g.51521259C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62444C=
NR_135237.1:n.694+62444C=