Canonical Allele Identifier: CA769932091
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1388739546
MyVariant Identifiers: chr2:g.52072501del (hg19) chr2:g.51845363del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845363del , CM000664.2:g.51845363del GRCh38
NC_000002.11:g.52072501del , CM000664.1:g.52072501del GRCh37
NC_000002.10:g.51926005del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16086del
NR_135237.1:n.840-16086del
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