Canonical Allele Identifier: CA769945775
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1313976393
MyVariant Identifiers: chr2:g.52163226_52163227insTATACG (hg19) chr2:g.51936088_51936089insTATACG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936089_51936090insATACGT , CM000664.2:g.51936089_51936090insATACGT GRCh38
NC_000002.11:g.52163227_52163228insATACGT , CM000664.1:g.52163227_52163228insATACGT GRCh37
NC_000002.10:g.52016731_52016732insATACGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74601_879+74602insATACGT
NR_135237.1:n.879+74601_879+74602insATACGT
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