Canonical Allele Identifier: CA769932108

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1393026279
• gnomAD v3: 2-51845386-T-C
• gnomAD v4: 2-51845386-T-C
• MyVariant Identifiers: chr2:g.52072524T>C (hg19) ; chr2:g.51845386T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845386T>C , CM000664.2:g.51845386T>C	GRCh38
NC_000002.11:g.52072524T>C , CM000664.1:g.52072524T>C	GRCh37
NC_000002.10:g.51926028T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16063T>C
NR_135237.1:n.840-16063T>C