Canonical Allele Identifier: CA532709325
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1168174367
gnomAD v2: 2-52163224-A-ACG
gnomAD v3: 2-51936086-A-ACG
gnomAD v4: 2-51936086-A-ACG
MyVariant Identifiers: chr2:g.52163224_52163225insCG (hg19) chr2:g.51936086_51936087insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936086_51936087insCG , CM000664.2:g.51936086_51936087insCG GRCh38
NC_000002.11:g.52163224_52163225insCG , CM000664.1:g.52163224_52163225insCG GRCh37
NC_000002.10:g.52016728_52016729insCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.879+74598_879+74599insCG
NR_135237.1:n.879+74598_879+74599insCG
Search 100 bp 5'
Search 100 bp 3'