Canonical Allele Identifier: CA48266036
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1020869882
gnomAD v2: 2-52162977-G-A
gnomAD v3: 2-51935839-G-A
gnomAD v4: 2-51935839-G-A
MyVariant Identifiers: chr2:g.52162977G>A (hg19) chr2:g.51935839G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935839G>A , CM000664.2:g.51935839G>A GRCh38
NC_000002.11:g.52162977G>A , CM000664.1:g.52162977G>A GRCh37
NC_000002.10:g.52016481G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74351G>A
NR_135237.1:n.879+74351G>A
Search 100 bp 5'
Search 100 bp 3'