Canonical Allele Identifier: CA532694308
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1277883141
gnomAD v2: 2-52072152-A-AT
gnomAD v3: 2-51845014-A-AT
gnomAD v4: 2-51845014-A-AT
MyVariant Identifiers: chr2:g.52072152_52072153insT (hg19) chr2:g.51845014_51845015insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845019dup , CM000664.2:g.51845019dup GRCh38
NC_000002.11:g.52072157dup , CM000664.1:g.52072157dup GRCh37
NC_000002.10:g.51925661dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16430dup
NR_135237.1:n.840-16430dup
Search 100 bp 5'
Search 100 bp 3'