Canonical Allele Identifier: CA532709153
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1356583596
gnomAD v2: 2-52163120-C-A
gnomAD v3: 2-51935982-C-A
gnomAD v4: 2-51935982-C-A
MyVariant Identifiers: chr2:g.52163120C>A (hg19) chr2:g.51935982C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935982C>A , CM000664.2:g.51935982C>A GRCh38
NC_000002.11:g.52163120C>A , CM000664.1:g.52163120C>A GRCh37
NC_000002.10:g.52016624C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74494C>A
NR_135237.1:n.879+74494C>A
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