Canonical Allele Identifier: CA532709149
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1302442138
gnomAD v2: 2-52163061-T-TG
gnomAD v3: 2-51935923-T-TG
gnomAD v4: 2-51935923-T-TG
MyVariant Identifiers: chr2:g.52163061_52163062insG (hg19) chr2:g.51935923_51935924insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935927dup , CM000664.2:g.51935927dup GRCh38
NC_000002.11:g.52163065dup , CM000664.1:g.52163065dup GRCh37
NC_000002.10:g.52016569dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74439dup
NR_135237.1:n.879+74439dup
Search 100 bp 5'
Search 100 bp 3'