Canonical Allele Identifier: CA1030641198
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667865098
gnomAD v3: 2-51936113-A-T
gnomAD v4: 2-51936113-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936113A>T , CM000664.2:g.51936113A>T GRCh38
NC_000002.11:g.52163251A>T , CM000664.1:g.52163251A>T GRCh37
NC_000002.10:g.52016755A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74625A>T
NR_135237.1:n.879+74625A>T