Canonical Allele Identifier: CA48253030

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs957236986
• gnomAD v3: 2-51845017-T-A
• gnomAD v4: 2-51845017-T-A
• MyVariant Identifiers: chr2:g.52072155T>A (hg19) ; chr2:g.51845017T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845017T>A , CM000664.2:g.51845017T>A	GRCh38
NC_000002.11:g.52072155T>A , CM000664.1:g.52072155T>A	GRCh37
NC_000002.10:g.51925659T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16432T>A
NR_135237.1:n.840-16432T>A