Canonical Allele Identifier: CA532709206
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667852153
gnomAD v2: 2-52163154-ATATGTATATATATATACGTATATATATATATG-A
gnomAD v3: 2-51936016-ATATGTATATATATATACGTATATATATATATG-A
gnomAD v4: 2-51936016-ATATGTATATATATATACGTATATATATATATG-A
MyVariant Identifiers: chr2:g.52163158_52163228delinsATATATATATGTATATATATATATGTATATATATATATG (hg19) chr2:g.51936020_51936090delinsATATATATATGTATATATATATATGTATATATATATATG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936020_51936051del , CM000664.2:g.51936020_51936051del GRCh38
NC_000002.11:g.52163158_52163189del , CM000664.1:g.52163158_52163189del GRCh37
NC_000002.10:g.52016662_52016693del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74532_879+74563del
NR_135237.1:n.879+74532_879+74563del
Search 100 bp 5'
Search 100 bp 3'