Canonical Allele Identifier: CA2597942520
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103743987
gnomAD v3: 2-51440615-T-C
gnomAD v4: 2-51440615-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440615T>C , CM000664.2:g.51440615T>C GRCh38
NC_000002.11:g.51667753T>C , CM000664.1:g.51667753T>C GRCh37
NC_000002.10:g.51521257T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62442T>C
NR_135237.1:n.694+62442T>C