Canonical Allele Identifier: CA2570797182
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935780A>G , CM000664.2:g.51935780A>G GRCh38
NC_000002.11:g.52162918A>G , CM000664.1:g.52162918A>G GRCh37
NC_000002.10:g.52016422A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74292A>G
NR_135237.1:n.879+74292A>G