Canonical Allele Identifier: CA48166606
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1206397
gnomAD v2: 2-51667739-C-A
gnomAD v3: 2-51440601-C-A
gnomAD v4: 2-51440601-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440601C>A , CM000664.2:g.51440601C>A GRCh38
NC_000002.11:g.51667739C>A , CM000664.1:g.51667739C>A GRCh37
NC_000002.10:g.51521243C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62428C>A
NR_135237.1:n.694+62428C>A