Canonical Allele Identifier: CA532694357
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1449187749
gnomAD v2: 2-52072554-A-G
gnomAD v3: 2-51845416-A-G
gnomAD v4: 2-51845416-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845416A>G , CM000664.2:g.51845416A>G GRCh38
NC_000002.11:g.52072554A>G , CM000664.1:g.52072554A>G GRCh37
NC_000002.10:g.51926058A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16033A>G
NR_135237.1:n.840-16033A>G