Canonical Allele Identifier: CA532669763

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1436571013
• gnomAD v2: 2-51667735-A-G
• gnomAD v3: 2-51440597-A-G
• gnomAD v4: 2-51440597-A-G
• MyVariant Identifiers: chr2:g.51667735A>G (hg19) ; chr2:g.51440597A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51440597A>G , CM000664.2:g.51440597A>G	GRCh38
NC_000002.11:g.51667735A>G , CM000664.1:g.51667735A>G	GRCh37
NC_000002.10:g.51521239A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.694+62424A>G
NR_135237.1:n.694+62424A>G