Canonical Allele Identifier: CA769932135
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs915721866
MyVariant Identifiers: chr2:g.52072553G>A (hg19) chr2:g.51845415G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845415G>A , CM000664.2:g.51845415G>A GRCh38
NC_000002.11:g.52072553G>A , CM000664.1:g.52072553G>A GRCh37
NC_000002.10:g.51926057G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16034G>A
NR_135237.1:n.840-16034G>A
Search 100 bp 5'
Search 100 bp 3'