Canonical Allele Identifier: CA48253102
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs869040769
MyVariant Identifiers: chr2:g.52072619_52072620insT (hg19) chr2:g.51845481_51845482insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845481_51845482insT , CM000664.2:g.51845481_51845482insT GRCh38
NC_000002.11:g.52072619_52072620insT , CM000664.1:g.52072619_52072620insT GRCh37
NC_000002.10:g.51926123_51926124insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15968_840-15967insT
NR_135237.1:n.840-15968_840-15967insT
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