Canonical Allele Identifier: CA48266027
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1001595093
MyVariant Identifiers: chr2:g.52162925T>C (hg19) chr2:g.51935787T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935787T>C , CM000664.2:g.51935787T>C GRCh38
NC_000002.11:g.52162925T>C , CM000664.1:g.52162925T>C GRCh37
NC_000002.10:g.52016429T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74299T>C
NR_135237.1:n.879+74299T>C
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