Canonical Allele Identifier: CA532709331
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1333301255
gnomAD v2: 2-52163230-A-G
gnomAD v3: 2-51936092-A-G
gnomAD v4: 2-51936092-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936092A>G , CM000664.2:g.51936092A>G GRCh38
NC_000002.11:g.52163230A>G , CM000664.1:g.52163230A>G GRCh37
NC_000002.10:g.52016734A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74604A>G
NR_135237.1:n.879+74604A>G