Canonical Allele Identifier: CA48266113
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs539675163
gnomAD v2: 2-52163411-G-T
gnomAD v3: 2-51936273-G-T
gnomAD v4: 2-51936273-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936273G>T , CM000664.2:g.51936273G>T GRCh38
NC_000002.11:g.52163411G>T , CM000664.1:g.52163411G>T GRCh37
NC_000002.10:g.52016915G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74785G>T
NR_135237.1:n.879+74785G>T