Canonical Allele Identifier: CA532709144
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1216683806
gnomAD v2: 2-52162932-G-C
gnomAD v3: 2-51935794-G-C
gnomAD v4: 2-51935794-G-C
MyVariant Identifiers: chr2:g.52162932G>C (hg19) chr2:g.51935794G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935794G>C , CM000664.2:g.51935794G>C GRCh38
NC_000002.11:g.52162932G>C , CM000664.1:g.52162932G>C GRCh37
NC_000002.10:g.52016436G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74306G>C
NR_135237.1:n.879+74306G>C
Search 100 bp 5'
Search 100 bp 3'