Canonical Allele Identifier: CA769932179
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1341860617
gnomAD v3: 2-51845505-ATGATT-A
gnomAD v4: 2-51845505-ATGATT-A
MyVariant Identifiers: chr2:g.52072644_52072648del (hg19) chr2:g.51845506_51845510del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845508_51845512del , CM000664.2:g.51845508_51845512del GRCh38
NC_000002.11:g.52072646_52072650del , CM000664.1:g.52072646_52072650del GRCh37
NC_000002.10:g.51926150_51926154del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15941_840-15937del
NR_135237.1:n.840-15941_840-15937del
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