Canonical Allele Identifier: CA2699183719
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103743875

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440504A>T , CM000664.2:g.51440504A>T GRCh38
NC_000002.11:g.51667642A>T , CM000664.1:g.51667642A>T GRCh37
NC_000002.10:g.51521146A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.694+62331A>T
NR_135237.1:n.694+62331A>T