Canonical Allele Identifier: CA2500376659
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845075A>G , CM000664.2:g.51845075A>G GRCh38
NC_000002.11:g.52072213A>G , CM000664.1:g.52072213A>G GRCh37
NC_000002.10:g.51925717A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16374A>G
NR_135237.1:n.840-16374A>G