Canonical Allele Identifier: CA11250219
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51509856C>T , CM000664.2:g.51509856C>T GRCh38
NC_000002.11:g.51736994C>T , CM000664.1:g.51736994C>T GRCh37
NC_000002.10:g.51590498C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.695-17746C>T
NR_135237.1:n.695-17746C>T