Canonical Allele Identifier: CA48253040

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs975010606
• MyVariant Identifiers: chr2:g.52072207C>T (hg19) ; chr2:g.51845069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845069C>T , CM000664.2:g.51845069C>T	GRCh38
NC_000002.11:g.52072207C>T , CM000664.1:g.52072207C>T	GRCh37
NC_000002.10:g.51925711C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16380C>T
NR_135237.1:n.840-16380C>T