Canonical Allele Identifier: CA769932006
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1222594525
gnomAD v3: 2-51845213-A-T
gnomAD v4: 2-51845213-A-T
MyVariant Identifiers: chr2:g.52072351A>T (hg19) chr2:g.51845213A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845213A>T , CM000664.2:g.51845213A>T GRCh38
NC_000002.11:g.52072351A>T , CM000664.1:g.52072351A>T GRCh37
NC_000002.10:g.51925855A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.840-16236A>T
NR_135237.1:n.840-16236A>T
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