Canonical Allele Identifier: CA532694365
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1333829301
gnomAD v2: 2-52072611-C-T
gnomAD v3: 2-51845473-C-T
gnomAD v4: 2-51845473-C-T
MyVariant Identifiers: chr2:g.52072611C>T (hg19) chr2:g.51845473C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845473C>T , CM000664.2:g.51845473C>T GRCh38
NC_000002.11:g.52072611C>T , CM000664.1:g.52072611C>T GRCh37
NC_000002.10:g.51926115C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15976C>T
NR_135237.1:n.840-15976C>T
Search 100 bp 5'
Search 100 bp 3'