Canonical Allele Identifier: CA1030637392
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667843195
gnomAD v3: 2-51935801-A-C
gnomAD v4: 2-51935801-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935801A>C , CM000664.2:g.51935801A>C GRCh38
NC_000002.11:g.52162939A>C , CM000664.1:g.52162939A>C GRCh37
NC_000002.10:g.52016443A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74313A>C
NR_135237.1:n.879+74313A>C