Canonical Allele Identifier: CA2148683625
Community Standard Title: NC_000014.9:g.78068563G=
Gene: NRXN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.78068563G= , CM000676.2:g.78068563G= GRCh38
NC_000014.8:g.78534906G= , CM000676.1:g.78534906G= GRCh37
NC_000014.7:g.77604659G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537364.1:c.-704+6242G= XP_011535666.1:n.-704+6242G=
XM_011537364.2:c.-704+6242G= XP_011535666.1:n.-704+6242G=
XM_017021790.1:c.-704+6242G= XP_016877279.1:n.-704+6242G=
XM_017021791.1:c.-704+6242G= XP_016877280.1:n.-704+6242G=