Canonical Allele Identifier: CA646660972
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667866760
gnomAD v3: 2-51936237-C-G
gnomAD v4: 2-51936237-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936237C>G , CM000664.2:g.51936237C>G GRCh38
NC_000002.11:g.52163375C>G , CM000664.1:g.52163375C>G GRCh37
NC_000002.10:g.52016879C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74749C>G
NR_135237.1:n.879+74749C>G