Canonical Allele Identifier: CA48253094
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1032792458
MyVariant Identifiers: chr2:g.51845426G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845426G>C , CM000664.2:g.51845426G>C GRCh38
NC_000002.11:g.52072564G>C , CM000664.1:g.52072564G>C GRCh37
NC_000002.10:g.51926068G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16023G>C
NR_135237.1:n.840-16023G>C