Canonical Allele Identifier: CA769945958
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1299523666
gnomAD v3: 2-51936246-G-T
gnomAD v4: 2-51936246-G-T
MyVariant Identifiers: chr2:g.52163384G>T (hg19) chr2:g.51936246G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936246G>T , CM000664.2:g.51936246G>T GRCh38
NC_000002.11:g.52163384G>T , CM000664.1:g.52163384G>T GRCh37
NC_000002.10:g.52016888G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74758G>T
NR_135237.1:n.879+74758G>T
Search 100 bp 5'
Search 100 bp 3'