Canonical Allele Identifier: CA769944545
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1486307065
MyVariant Identifiers: chr2:g.52162940G>A (hg19) chr2:g.51935802G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935802G>A , CM000664.2:g.51935802G>A GRCh38
NC_000002.11:g.52162940G>A , CM000664.1:g.52162940G>A GRCh37
NC_000002.10:g.52016444G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74314G>A
NR_135237.1:n.879+74314G>A
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