Canonical Allele Identifier: CA769874662
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1168848837
MyVariant Identifiers: chr2:g.51667815_51667823del (hg19) chr2:g.51440677_51440685del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440680_51440688del , CM000664.2:g.51440680_51440688del GRCh38
NC_000002.11:g.51667818_51667826del , CM000664.1:g.51667818_51667826del GRCh37
NC_000002.10:g.51521322_51521330del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.694+62507_694+62515del
NR_135237.1:n.694+62507_694+62515del
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