Canonical Allele Identifier: CA532709148
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1434103870
gnomAD v2: 2-52162962-G-A
gnomAD v3: 2-51935824-G-A
gnomAD v4: 2-51935824-G-A
MyVariant Identifiers: chr2:g.52162962G>A (hg19) chr2:g.51935824G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935824G>A , CM000664.2:g.51935824G>A GRCh38
NC_000002.11:g.52162962G>A , CM000664.1:g.52162962G>A GRCh37
NC_000002.10:g.52016466G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74336G>A
NR_135237.1:n.879+74336G>A
Search 100 bp 5'
Search 100 bp 3'