Canonical Allele Identifier: CA769945885
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1465918418
gnomAD v3: 2-51936100-A-G
gnomAD v4: 2-51936100-A-G
MyVariant Identifiers: chr2:g.52163238A>G (hg19) chr2:g.51936100A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936100A>G , CM000664.2:g.51936100A>G GRCh38
NC_000002.11:g.52163238A>G , CM000664.1:g.52163238A>G GRCh37
NC_000002.10:g.52016742A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74612A>G
NR_135237.1:n.879+74612A>G
Search 100 bp 5'
Search 100 bp 3'