Canonical Allele Identifier: CA769944854
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1161081936
MyVariant Identifiers: chr2:g.52163145_52163148del (hg19) chr2:g.51936007_51936010del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936016_51936019del , CM000664.2:g.51936016_51936019del GRCh38
NC_000002.11:g.52163154_52163157del , CM000664.1:g.52163154_52163157del GRCh37
NC_000002.10:g.52016658_52016661del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74528_879+74531del
NR_135237.1:n.879+74528_879+74531del
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