Canonical Allele Identifier: CA1250398150
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936174A= , CM000664.2:g.51936174A= GRCh38
NC_000002.11:g.52163312A= , CM000664.1:g.52163312A= GRCh37
NC_000002.10:g.52016816A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74686A=
NR_135237.1:n.879+74686A=