Canonical Allele Identifier: CA532669771

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1427905097
• gnomAD v2: 2-51667895-C-T
• gnomAD v3: 2-51440757-C-T
• gnomAD v4: 2-51440757-C-T
• MyVariant Identifiers: chr2:g.51667895C>T (hg19) ; chr2:g.51440757C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51440757C>T , CM000664.2:g.51440757C>T	GRCh38
NC_000002.11:g.51667895C>T , CM000664.1:g.51667895C>T	GRCh37
NC_000002.10:g.51521399C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.694+62584C>T
NR_135237.1:n.694+62584C>T