Canonical Allele Identifier: CA769932197
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1410250195
MyVariant Identifiers: chr2:g.52072677C>T (hg19) chr2:g.51845539C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845539C>T , CM000664.2:g.51845539C>T GRCh38
NC_000002.11:g.52072677C>T , CM000664.1:g.52072677C>T GRCh37
NC_000002.10:g.51926181C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15910C>T
NR_135237.1:n.840-15910C>T
Search 100 bp 5'
Search 100 bp 3'