Canonical Allele Identifier: CA1250344722
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs182098496

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845074C>G , CM000664.2:g.51845074C>G GRCh38
NC_000002.11:g.52072212C>G , CM000664.1:g.52072212C>G GRCh37
NC_000002.10:g.51925716C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16375C>G
NR_135237.1:n.840-16375C>G