Canonical Allele Identifier: CA2749903741
Gene: NRXN1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440605A>C , CM000664.2:g.51440605A>C GRCh38
NC_000002.11:g.51667743A>C , CM000664.1:g.51667743A>C GRCh37
NC_000002.10:g.51521247A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62432A>C
NR_135237.1:n.694+62432A>C