Canonical Allele Identifier: CA1250398221
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667867007

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936250G>T , CM000664.2:g.51936250G>T GRCh38
NC_000002.11:g.52163388G>T , CM000664.1:g.52163388G>T GRCh37
NC_000002.10:g.52016892G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74762G>T
NR_135237.1:n.879+74762G>T