Canonical Allele Identifier: CA2148683624
Gene: NRXN3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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