Canonical Allele Identifier: CA1250398256
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667867524
gnomAD v3: 2-51936275-G-T
gnomAD v4: 2-51936275-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936275G>T , CM000664.2:g.51936275G>T GRCh38
NC_000002.11:g.52163413G>T , CM000664.1:g.52163413G>T GRCh37
NC_000002.10:g.52016917G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74787G>T
NR_135237.1:n.879+74787G>T