Canonical Allele Identifier: CA48253062
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs913129354
MyVariant Identifiers: chr2:g.52072350C>A (hg19) chr2:g.51845212C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845212C>A , CM000664.2:g.51845212C>A GRCh38
NC_000002.11:g.52072350C>A , CM000664.1:g.52072350C>A GRCh37
NC_000002.10:g.51925854C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16237C>A
NR_135237.1:n.840-16237C>A
Search 100 bp 5'
Search 100 bp 3'