Canonical Allele Identifier: CA769874617
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1307002040
gnomAD v3: 2-51440625-C-T
gnomAD v4: 2-51440625-C-T
MyVariant Identifiers: chr2:g.51667763C>T (hg19) chr2:g.51440625C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440625C>T , CM000664.2:g.51440625C>T GRCh38
NC_000002.11:g.51667763C>T , CM000664.1:g.51667763C>T GRCh37
NC_000002.10:g.51521267C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62452C>T
NR_135237.1:n.694+62452C>T
Search 100 bp 5'
Search 100 bp 3'