Canonical Allele Identifier: CA1030641427
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1380073506
gnomAD v3: 2-51936135-A-G
gnomAD v4: 2-51936135-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936135A>G , CM000664.2:g.51936135A>G GRCh38
NC_000002.11:g.52163273A>G , CM000664.1:g.52163273A>G GRCh37
NC_000002.10:g.52016777A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74647A>G
NR_135237.1:n.879+74647A>G