Canonical Allele Identifier: CA2598001685
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103758525
gnomAD v3: 2-51935781-G-C
gnomAD v4: 2-51935781-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935781G>C , CM000664.2:g.51935781G>C GRCh38
NC_000002.11:g.52162919G>C , CM000664.1:g.52162919G>C GRCh37
NC_000002.10:g.52016423G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74293G>C
NR_135237.1:n.879+74293G>C