Canonical Allele Identifier: CA2699188117
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103647170

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51844902A>G , CM000664.2:g.51844902A>G GRCh38
NC_000002.11:g.52072040A>G , CM000664.1:g.52072040A>G GRCh37
NC_000002.10:g.51925544A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16547A>G
NR_135237.1:n.840-16547A>G