Canonical Allele Identifier: CA532693679
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1279374709
gnomAD v2: 2-51959158-A-G
gnomAD v3: 2-51732020-A-G
gnomAD v4: 2-51732020-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732020A>G , CM000664.2:g.51732020A>G GRCh38
NC_000002.11:g.51959158A>G , CM000664.1:g.51959158A>G GRCh37
NC_000002.10:g.51812662A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30069A>G
NR_135237.1:n.754-30069A>G