Canonical Allele Identifier: CA48266047

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs940425818
• gnomAD v4: 2-51935916-G-T
• MyVariant Identifiers: chr2:g.52163054G>T (hg19) ; chr2:g.51935916G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51935916G>T , CM000664.2:g.51935916G>T	GRCh38
NC_000002.11:g.52163054G>T , CM000664.1:g.52163054G>T	GRCh37
NC_000002.10:g.52016558G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74428G>T
NR_135237.1:n.879+74428G>T