Canonical Allele Identifier: CA264048609
Gene: NRXN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.78063343G>A , CM000676.2:g.78063343G>A GRCh38
NC_000014.8:g.78529686G>A , CM000676.1:g.78529686G>A GRCh37
NC_000014.7:g.77599439G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537364.1:c.-704+1022G>A XP_011535666.1:n.-704+1022G>A
XM_011537364.2:c.-704+1022G>A XP_011535666.1:n.-704+1022G>A
XM_017021790.1:c.-704+1022G>A XP_016877279.1:n.-704+1022G>A
XM_017021791.1:c.-704+1022G>A XP_016877280.1:n.-704+1022G>A