Canonical Allele Identifier: CA769874618
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1488661982
MyVariant Identifiers: chr2:g.51667766A>T (hg19) chr2:g.51440628A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440628A>T , CM000664.2:g.51440628A>T GRCh38
NC_000002.11:g.51667766A>T , CM000664.1:g.51667766A>T GRCh37
NC_000002.10:g.51521270A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62455A>T
NR_135237.1:n.694+62455A>T
Search 100 bp 5'
Search 100 bp 3'