Canonical Allele Identifier: CA48266107
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1029209632
MyVariant Identifiers: chr2:g.52163385A>G (hg19) chr2:g.51936247A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936247A>G , CM000664.2:g.51936247A>G GRCh38
NC_000002.11:g.52163385A>G , CM000664.1:g.52163385A>G GRCh37
NC_000002.10:g.52016889A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74759A>G
NR_135237.1:n.879+74759A>G
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