Canonical Allele Identifier: CA1250396873
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667842364

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935763A>C , CM000664.2:g.51935763A>C GRCh38
NC_000002.11:g.52162901A>C , CM000664.1:g.52162901A>C GRCh37
NC_000002.10:g.52016405A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74275A>C
NR_135237.1:n.879+74275A>C