Canonical Allele Identifier: CA1030641217
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103760219
gnomAD v3: 2-51936115-T-A
gnomAD v4: 2-51936115-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936115T>A , CM000664.2:g.51936115T>A GRCh38
NC_000002.11:g.52163253T>A , CM000664.1:g.52163253T>A GRCh37
NC_000002.10:g.52016757T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74627T>A
NR_135237.1:n.879+74627T>A