Canonical Allele Identifier: CA426114961
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1254826750
gnomAD v2: 2-52163228-G-GTA
gnomAD v3: 2-51936090-G-GTA
gnomAD v4: 2-51936090-G-GTA
MyVariant Identifiers: chr2:g.52163230_52163231insTA (hg19) chr2:g.52163228_52163229insTA (hg19) chr2:g.51936092_51936093insTA (hg38) chr2:g.51936090_51936091insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936100_51936101dup , CM000664.2:g.51936100_51936101dup GRCh38
NC_000002.11:g.52163238_52163239dup , CM000664.1:g.52163238_52163239dup GRCh37
NC_000002.10:g.52016742_52016743dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74612_879+74613dup
NR_135237.1:n.879+74612_879+74613dup
Search 100 bp 5'
Search 100 bp 3'