Canonical Allele Identifier: CA769874631

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1219792140
• gnomAD v3: 2-51440646-T-C
• gnomAD v4: 2-51440646-T-C
• MyVariant Identifiers: chr2:g.51667784T>C (hg19) ; chr2:g.51440646T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51440646T>C , CM000664.2:g.51440646T>C	GRCh38
NC_000002.11:g.51667784T>C , CM000664.1:g.51667784T>C	GRCh37
NC_000002.10:g.51521288T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245003.1:n.694+62473T>C
NR_135237.1:n.694+62473T>C