Canonical Allele Identifier: CA532709199
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1274324368
gnomAD v2: 2-52163152-ATATATGTATATATATATACGTATATATATATATG-A
gnomAD v3: 2-51936014-ATATATGTATATATATATACGTATATATATATATG-A
gnomAD v4: 2-51936014-ATATATGTATATATATATACGTATATATATATATG-A
MyVariant Identifiers: chr2:g.52163153_52163186del (hg19) chr2:g.52163158_52163228delinsATATATATGTATATATATATATGTATATATATATATG (hg19) chr2:g.51936015_51936048del (hg38) chr2:g.51936020_51936090delinsATATATATGTATATATATATATGTATATATATATATG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936020_51936053del , CM000664.2:g.51936020_51936053del GRCh38
NC_000002.11:g.52163158_52163191del , CM000664.1:g.52163158_52163191del GRCh37
NC_000002.10:g.52016662_52016695del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74532_879+74565del
NR_135237.1:n.879+74532_879+74565del
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Search 100 bp 3'