Canonical Allele Identifier: CA48266098

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs893261984
• gnomAD v3: 2-51936144-C-G
• gnomAD v4: 2-51936144-C-G
• MyVariant Identifiers: chr2:g.52163282C>G (hg19) ; chr2:g.51936144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51936144C>G , CM000664.2:g.51936144C>G	GRCh38
NC_000002.11:g.52163282C>G , CM000664.1:g.52163282C>G	GRCh37
NC_000002.10:g.52016786C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74656C>G
NR_135237.1:n.879+74656C>G