Canonical Allele Identifier: CA2538151082
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935779T>C , CM000664.2:g.51935779T>C GRCh38
NC_000002.11:g.52162917T>C , CM000664.1:g.52162917T>C GRCh37
NC_000002.10:g.52016421T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74291T>C
NR_135237.1:n.879+74291T>C