Canonical Allele Identifier: CA1250397052
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667844883

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935912G>C , CM000664.2:g.51935912G>C GRCh38
NC_000002.11:g.52163050G>C , CM000664.1:g.52163050G>C GRCh37
NC_000002.10:g.52016554G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74424G>C
NR_135237.1:n.879+74424G>C