Canonical Allele Identifier: CA48253078
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs749231052
gnomAD v2: 2-52072466-G-C
gnomAD v3: 2-51845328-G-C
gnomAD v4: 2-51845328-G-C
MyVariant Identifiers: chr2:g.52072466G>C (hg19) chr2:g.51845328G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845328G>C , CM000664.2:g.51845328G>C GRCh38
NC_000002.11:g.52072466G>C , CM000664.1:g.52072466G>C GRCh37
NC_000002.10:g.51925970G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16121G>C
NR_135237.1:n.840-16121G>C
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