Canonical Allele Identifier: CA11152002
Gene: NRXN1-DT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51725011G>A , CM000664.2:g.51725011G>A GRCh38
NC_000002.11:g.51952149G>A , CM000664.1:g.51952149G>A GRCh37
NC_000002.10:g.51805653G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-37078G>A
NR_135237.1:n.754-37078G>A
Search 100 bp 5'
Search 100 bp 3'