Canonical Allele Identifier: CA1030641213
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667865132
gnomAD v3: 2-51936114-G-A
gnomAD v4: 2-51936114-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936114G>A , CM000664.2:g.51936114G>A GRCh38
NC_000002.11:g.52163252G>A , CM000664.1:g.52163252G>A GRCh37
NC_000002.10:g.52016756G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74626G>A
NR_135237.1:n.879+74626G>A