Canonical Allele Identifier: CA1030634792
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671963571
gnomAD v3: 2-51845511-T-C
gnomAD v4: 2-51845511-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845511T>C , CM000664.2:g.51845511T>C GRCh38
NC_000002.11:g.52072649T>C , CM000664.1:g.52072649T>C GRCh37
NC_000002.10:g.51926153T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15938T>C
NR_135237.1:n.840-15938T>C