Canonical Allele Identifier: CA48266116
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs78659491
gnomAD v2: 2-52163433-T-G
gnomAD v3: 2-51936295-T-G
gnomAD v4: 2-51936295-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936295T>G , CM000664.2:g.51936295T>G GRCh38
NC_000002.11:g.52163433T>G , CM000664.1:g.52163433T>G GRCh37
NC_000002.10:g.52016937T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74807T>G
NR_135237.1:n.879+74807T>G