Canonical Allele Identifier: CA2699118115
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1448908878

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845030C>G , CM000664.2:g.51845030C>G GRCh38
NC_000002.11:g.52072168C>G , CM000664.1:g.52072168C>G GRCh37
NC_000002.10:g.51925672C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.840-16419C>G
NR_135237.1:n.840-16419C>G