Canonical Allele Identifier: CA1250344798
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845213A= , CM000664.2:g.51845213A= GRCh38
NC_000002.11:g.52072351A= , CM000664.1:g.52072351A= GRCh37
NC_000002.10:g.51925855A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16236A=
NR_135237.1:n.840-16236A=