Canonical Allele Identifier: CA769945850
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1333301255
gnomAD v3: 2-51936092-A-C
gnomAD v4: 2-51936092-A-C
MyVariant Identifiers: chr2:g.52163230A>C (hg19) chr2:g.51936092A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936092A>C , CM000664.2:g.51936092A>C GRCh38
NC_000002.11:g.52163230A>C , CM000664.1:g.52163230A>C GRCh37
NC_000002.10:g.52016734A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74604A>C
NR_135237.1:n.879+74604A>C
Search 100 bp 5'
Search 100 bp 3'