Canonical Allele Identifier: CA769944646
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs905878105
gnomAD v3: 2-51935970-G-C
gnomAD v4: 2-51935970-G-C
MyVariant Identifiers: chr2:g.52163108G>C (hg19) chr2:g.51935970G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51935970G>C , CM000664.2:g.51935970G>C GRCh38
NC_000002.11:g.52163108G>C , CM000664.1:g.52163108G>C GRCh37
NC_000002.10:g.52016612G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74482G>C
NR_135237.1:n.879+74482G>C
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