Canonical Allele Identifier: CA48253031

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs146810285
• gnomAD v2: 2-52072158-A-G
• gnomAD v3: 2-51845020-A-G
• gnomAD v4: 2-51845020-A-G
• MyVariant Identifiers: chr2:g.52072158A>G (hg19) ; chr2:g.51845020A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845020A>G , CM000664.2:g.51845020A>G	GRCh38
NC_000002.11:g.52072158A>G , CM000664.1:g.52072158A>G	GRCh37
NC_000002.10:g.51925662A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16429A>G
NR_135237.1:n.840-16429A>G