Canonical Allele Identifier: CA769944568
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1020869882
gnomAD v3: 2-51935839-G-C
gnomAD v4: 2-51935839-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935839G>C , CM000664.2:g.51935839G>C GRCh38
NC_000002.11:g.52162977G>C , CM000664.1:g.52162977G>C GRCh37
NC_000002.10:g.52016481G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74351G>C
NR_135237.1:n.879+74351G>C