Canonical Allele Identifier: CA769932152
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1430666601
gnomAD v3: 2-51845453-G-A
gnomAD v4: 2-51845453-G-A
MyVariant Identifiers: chr2:g.52072591G>A (hg19) chr2:g.51845453G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845453G>A , CM000664.2:g.51845453G>A GRCh38
NC_000002.11:g.52072591G>A , CM000664.1:g.52072591G>A GRCh37
NC_000002.10:g.51926095G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15996G>A
NR_135237.1:n.840-15996G>A
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