Canonical Allele Identifier: CA1030634672
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671961788
gnomAD v3: 2-51845383-CTTTG-C
gnomAD v4: 2-51845383-CTTTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845387_51845390del , CM000664.2:g.51845387_51845390del GRCh38
NC_000002.11:g.52072525_52072528del , CM000664.1:g.52072525_52072528del GRCh37
NC_000002.10:g.51926029_51926032del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16062_840-16059del
NR_135237.1:n.840-16062_840-16059del
Search 100 bp 5'
Search 100 bp 3'