Canonical Allele Identifier: CA532709185

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1558530504
• gnomAD v2: 2-52163146-ATATATATATATGTATATATATATACGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATG-A
• gnomAD v3: 2-51936008-ATATATATATATGTATATATATATACGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATG-A
• gnomAD v4: 2-51936008-ATATATATATATGTATATATATATACGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATG-A
• MyVariant Identifiers: chr2:g.52163147_52163228del (hg19) ; chr2:g.51936009_51936090del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51936030_51936111del , CM000664.2:g.51936030_51936111del	GRCh38
NC_000002.11:g.52163168_52163249del , CM000664.1:g.52163168_52163249del	GRCh37
NC_000002.10:g.52016672_52016753del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74542_879+74623del
NR_135237.1:n.879+74542_879+74623del