Canonical Allele Identifier: CA1250397006
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667844736

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935904C>G , CM000664.2:g.51935904C>G GRCh38
NC_000002.11:g.52163042C>G , CM000664.1:g.52163042C>G GRCh37
NC_000002.10:g.52016546C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74416C>G
NR_135237.1:n.879+74416C>G