Canonical Allele Identifier: CA1250396901
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667842965

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935796G>A , CM000664.2:g.51935796G>A GRCh38
NC_000002.11:g.52162934G>A , CM000664.1:g.52162934G>A GRCh37
NC_000002.10:g.52016438G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74308G>A
NR_135237.1:n.879+74308G>A