Canonical Allele Identifier: CA2699188169
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103647950

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845455G>C , CM000664.2:g.51845455G>C GRCh38
NC_000002.11:g.52072593G>C , CM000664.1:g.52072593G>C GRCh37
NC_000002.10:g.51926097G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15994G>C
NR_135237.1:n.840-15994G>C