Canonical Allele Identifier: CA769932079

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1365889661
• gnomAD v3: 2-51845350-C-A
• gnomAD v4: 2-51845350-C-A
• MyVariant Identifiers: chr2:g.52072488C>A (hg19) ; chr2:g.51845350C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845350C>A , CM000664.2:g.51845350C>A	GRCh38
NC_000002.11:g.52072488C>A , CM000664.1:g.52072488C>A	GRCh37
NC_000002.10:g.51925992C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16099C>A
NR_135237.1:n.840-16099C>A