Canonical Allele Identifier: CA1250396862
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667842249

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935752T>C , CM000664.2:g.51935752T>C GRCh38
NC_000002.11:g.52162890T>C , CM000664.1:g.52162890T>C GRCh37
NC_000002.10:g.52016394T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74264T>C
NR_135237.1:n.879+74264T>C