Canonical Allele Identifier: CA2699190685
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103758646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935883G>A , CM000664.2:g.51935883G>A GRCh38
NC_000002.11:g.52163021G>A , CM000664.1:g.52163021G>A GRCh37
NC_000002.10:g.52016525G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74395G>A
NR_135237.1:n.879+74395G>A