Canonical Allele Identifier: CA769945921

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1392203883
• MyVariant Identifiers: chr2:g.52163310A>C (hg19) ; chr2:g.51936172A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51936172A>C , CM000664.2:g.51936172A>C	GRCh38
NC_000002.11:g.52163310A>C , CM000664.1:g.52163310A>C	GRCh37
NC_000002.10:g.52016814A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245003.1:n.879+74684A>C
NR_135237.1:n.879+74684A>C