Canonical Allele Identifier: CA48166628

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs891437978
• MyVariant Identifiers: chr2:g.51667853C>G (hg19) ; chr2:g.51440715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51440715C>G , CM000664.2:g.51440715C>G	GRCh38
NC_000002.11:g.51667853C>G , CM000664.1:g.51667853C>G	GRCh37
NC_000002.10:g.51521357C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.694+62542C>G
NR_135237.1:n.694+62542C>G