Canonical Allele Identifier: CA1030641092
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1403429081
gnomAD v3: 2-51936104-A-C
gnomAD v4: 2-51936104-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936104A>C , CM000664.2:g.51936104A>C GRCh38
NC_000002.11:g.52163242A>C , CM000664.1:g.52163242A>C GRCh37
NC_000002.10:g.52016746A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74616A>C
NR_135237.1:n.879+74616A>C