Canonical Allele Identifier: CA1250344782
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845188C= , CM000664.2:g.51845188C= GRCh38
NC_000002.11:g.52072326C= , CM000664.1:g.52072326C= GRCh37
NC_000002.10:g.51925830C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16261C=
NR_135237.1:n.840-16261C=