Canonical Allele Identifier: CA769945499
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1464772397
gnomAD v3: 2-51732052-C-T
gnomAD v4: 2-51732052-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732052C>T , CM000664.2:g.51732052C>T GRCh38
NC_000002.11:g.51959190C>T , CM000664.1:g.51959190C>T GRCh37
NC_000002.10:g.51812694C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30037C>T
NR_135237.1:n.754-30037C>T