Canonical Allele Identifier: CA1250344690
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671956770

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845023T>C , CM000664.2:g.51845023T>C GRCh38
NC_000002.11:g.52072161T>C , CM000664.1:g.52072161T>C GRCh37
NC_000002.10:g.51925665T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16426T>C
NR_135237.1:n.840-16426T>C