Canonical Allele Identifier: CA532709301
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1335027165
gnomAD v2: 2-52163202-ATATATATATATG-A
gnomAD v3: 2-51936064-ATATATATATATG-A
gnomAD v4: 2-51936064-ATATATATATATG-A
MyVariant Identifiers: chr2:g.52163203_52163214del (hg19) chr2:g.52163214_52163228delinsATG (hg19) chr2:g.51936065_51936076del (hg38) chr2:g.51936076_51936090delinsATG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936076_51936087del , CM000664.2:g.51936076_51936087del GRCh38
NC_000002.11:g.52163214_52163225del , CM000664.1:g.52163214_52163225del GRCh37
NC_000002.10:g.52016718_52016729del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74588_879+74599del
NR_135237.1:n.879+74588_879+74599del
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