Canonical Allele Identifier: CA48266035

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs939721249
• MyVariant Identifiers: chr2:g.52162974C>G (hg19) ; chr2:g.51935836C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51935836C>G , CM000664.2:g.51935836C>G	GRCh38
NC_000002.11:g.52162974C>G , CM000664.1:g.52162974C>G	GRCh37
NC_000002.10:g.52016478C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74348C>G
NR_135237.1:n.879+74348C>G