Canonical Allele Identifier: CA1030634531
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671958345
gnomAD v3: 2-51845132-T-C
gnomAD v4: 2-51845132-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845132T>C , CM000664.2:g.51845132T>C GRCh38
NC_000002.11:g.52072270T>C , CM000664.1:g.52072270T>C GRCh37
NC_000002.10:g.51925774T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.840-16317T>C
NR_135237.1:n.840-16317T>C