Canonical Allele Identifier: CA769945201

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1491105938
• MyVariant Identifiers: chr2:g.52163171_52163172insAT (hg19) ; chr2:g.51936033_51936034insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51936033_51936034insAT , CM000664.2:g.51936033_51936034insAT	GRCh38
NC_000002.11:g.52163171_52163172insAT , CM000664.1:g.52163171_52163172insAT	GRCh37
NC_000002.10:g.52016675_52016676insAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74545_879+74546insAT
NR_135237.1:n.879+74545_879+74546insAT