Canonical Allele Identifier: CA2699128273
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667866836

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936240C>T , CM000664.2:g.51936240C>T GRCh38
NC_000002.11:g.52163378C>T , CM000664.1:g.52163378C>T GRCh37
NC_000002.10:g.52016882C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74752C>T
NR_135237.1:n.879+74752C>T