Canonical Allele Identifier: CA48253081
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs941557686
MyVariant Identifiers: chr2:g.51845340A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845340A>G , CM000664.2:g.51845340A>G GRCh38
NC_000002.11:g.52072478A>G , CM000664.1:g.52072478A>G GRCh37
NC_000002.10:g.51925982A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16109A>G
NR_135237.1:n.840-16109A>G
Search 100 bp 5'
Search 100 bp 3'