Canonical Allele Identifier: CA1030634805
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1410250195
gnomAD v3: 2-51845539-C-G
gnomAD v4: 2-51845539-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845539C>G , CM000664.2:g.51845539C>G GRCh38
NC_000002.11:g.52072677C>G , CM000664.1:g.52072677C>G GRCh37
NC_000002.10:g.51926181C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15910C>G
NR_135237.1:n.840-15910C>G