Canonical Allele Identifier: CA48266025
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs564210630
gnomAD v2: 2-52162904-C-T
gnomAD v3: 2-51935766-C-T
gnomAD v4: 2-51935766-C-T
MyVariant Identifiers: chr2:g.52162904C>T (hg19) chr2:g.51935766C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935766C>T , CM000664.2:g.51935766C>T GRCh38
NC_000002.11:g.52162904C>T , CM000664.1:g.52162904C>T GRCh37
NC_000002.10:g.52016408C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74278C>T
NR_135237.1:n.879+74278C>T
Search 100 bp 5'
Search 100 bp 3'