Canonical Allele Identifier: CA48253092
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs773177815
gnomAD v2: 2-52072550-C-G
gnomAD v3: 2-51845412-C-G
gnomAD v4: 2-51845412-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845412C>G , CM000664.2:g.51845412C>G GRCh38
NC_000002.11:g.52072550C>G , CM000664.1:g.52072550C>G GRCh37
NC_000002.10:g.51926054C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16037C>G
NR_135237.1:n.840-16037C>G