Canonical Allele Identifier: CA1250344781
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671959017

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845186T>C , CM000664.2:g.51845186T>C GRCh38
NC_000002.11:g.52072324T>C , CM000664.1:g.52072324T>C GRCh37
NC_000002.10:g.51925828T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.840-16263T>C
NR_135237.1:n.840-16263T>C