Canonical Allele Identifier: CA48166614
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1048345002
MyVariant Identifiers: chr2:g.51667773T>C (hg19) chr2:g.51440635T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440635T>C , CM000664.2:g.51440635T>C GRCh38
NC_000002.11:g.51667773T>C , CM000664.1:g.51667773T>C GRCh37
NC_000002.10:g.51521277T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62462T>C
NR_135237.1:n.694+62462T>C
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