Canonical Allele Identifier: CA1250280007
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1669886818

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732032A>G , CM000664.2:g.51732032A>G GRCh38
NC_000002.11:g.51959170A>G , CM000664.1:g.51959170A>G GRCh37
NC_000002.10:g.51812674A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30057A>G
NR_135237.1:n.754-30057A>G