Canonical Allele Identifier: CA2699184020
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103760419

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936305A>G , CM000664.2:g.51936305A>G GRCh38
NC_000002.11:g.52163443A>G , CM000664.1:g.52163443A>G GRCh37
NC_000002.10:g.52016947A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74817A>G
NR_135237.1:n.879+74817A>G