Canonical Allele Identifier: CA769945588
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1533428
MyVariant Identifiers: chr2:g.51959258T>A (hg19) chr2:g.51732120T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732120T>A , CM000664.2:g.51732120T>A GRCh38
NC_000002.11:g.51959258T>A , CM000664.1:g.51959258T>A GRCh37
NC_000002.10:g.51812762T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.754-29969T>A
NR_135237.1:n.754-29969T>A
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