Canonical Allele Identifier: CA769932174
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1254448816
gnomAD v3: 2-51845489-TTAA-T
gnomAD v4: 2-51845489-TTAA-T
MyVariant Identifiers: chr2:g.52072628_52072630del (hg19) chr2:g.51845490_51845492del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845491_51845493del , CM000664.2:g.51845491_51845493del GRCh38
NC_000002.11:g.52072629_52072631del , CM000664.1:g.52072629_52072631del GRCh37
NC_000002.10:g.51926133_51926135del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15958_840-15956del
NR_135237.1:n.840-15958_840-15956del
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