Canonical Allele Identifier: CA769945476
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1378316302
gnomAD v3: 2-51732039-A-G
gnomAD v4: 2-51732039-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732039A>G , CM000664.2:g.51732039A>G GRCh38
NC_000002.11:g.51959177A>G , CM000664.1:g.51959177A>G GRCh37
NC_000002.10:g.51812681A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30050A>G
NR_135237.1:n.754-30050A>G