Canonical Allele Identifier: CA532709345
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1256832772
gnomAD v2: 2-52163388-GGACA-G
gnomAD v3: 2-51936250-GGACA-G
gnomAD v4: 2-51936250-GGACA-G
MyVariant Identifiers: chr2:g.52163389_52163392del (hg19) chr2:g.51936251_51936254del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936255_51936258del , CM000664.2:g.51936255_51936258del GRCh38
NC_000002.11:g.52163393_52163396del , CM000664.1:g.52163393_52163396del GRCh37
NC_000002.10:g.52016897_52016900del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74767_879+74770del
NR_135237.1:n.879+74767_879+74770del
Search 100 bp 5'
Search 100 bp 3'