Canonical Allele Identifier: CA48253106
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs900657325
MyVariant Identifiers: chr2:g.52072661C>T (hg19) chr2:g.51845523C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845523C>T , CM000664.2:g.51845523C>T GRCh38
NC_000002.11:g.52072661C>T , CM000664.1:g.52072661C>T GRCh37
NC_000002.10:g.51926165C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15926C>T
NR_135237.1:n.840-15926C>T
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