Canonical Allele Identifier: CA48236541
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs922241824
MyVariant Identifiers: chr2:g.51732049C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51732049C>G , CM000664.2:g.51732049C>G GRCh38
NC_000002.11:g.51959187C>G , CM000664.1:g.51959187C>G GRCh37
NC_000002.10:g.51812691C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.754-30040C>G
NR_135237.1:n.754-30040C>G