Canonical Allele Identifier: CA1250396852
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667842121

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935746A>T , CM000664.2:g.51935746A>T GRCh38
NC_000002.11:g.52162884A>T , CM000664.1:g.52162884A>T GRCh37
NC_000002.10:g.52016388A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74258A>T
NR_135237.1:n.879+74258A>T