Canonical Allele Identifier: CA48266048

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs777414790
• gnomAD v3: 2-51935916-GT-G
• gnomAD v4: 2-51935916-GT-G
• MyVariant Identifiers: chr2:g.52163055del (hg19) ; chr2:g.51935917del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51935921del , CM000664.2:g.51935921del	GRCh38
NC_000002.11:g.52163059del , CM000664.1:g.52163059del	GRCh37
NC_000002.10:g.52016563del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.879+74433del
NR_135237.1:n.879+74433del