Canonical Allele Identifier: CA532709280
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1558530701
gnomAD v2: 2-52163188-A-ATATATATATATGTATATATATATATGTATATATATATATG
gnomAD v3: 2-51936050-A-ATATATATATATGTATATATATATATGTATATATATATATG
gnomAD v4: 2-51936050-A-ATATATATATATGTATATATATATATGTATATATATATATG
MyVariant Identifiers: chr2:g.52163228_52163229insTATATATATATGTATATATATATATGTATATATATATATG (hg19) chr2:g.51936090_51936091insTATATATATATGTATATATATATATGTATATATATATATG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936072_51936111dup , CM000664.2:g.51936072_51936111dup GRCh38
NC_000002.11:g.52163210_52163249dup , CM000664.1:g.52163210_52163249dup GRCh37
NC_000002.10:g.52016714_52016753dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74584_879+74623dup
NR_135237.1:n.879+74584_879+74623dup
Search 100 bp 5'
Search 100 bp 3'