Canonical Allele Identifier: CA48266112

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs11889995
• gnomAD v2: 2-52163410-C-T
• gnomAD v3: 2-51936272-C-T
• gnomAD v4: 2-51936272-C-T
• MyVariant Identifiers: chr2:g.52163410C>T (hg19) ; chr2:g.51936272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51936272C>T , CM000664.2:g.51936272C>T	GRCh38
NC_000002.11:g.52163410C>T , CM000664.1:g.52163410C>T	GRCh37
NC_000002.10:g.52016914C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245003.1:n.879+74784C>T
NR_135237.1:n.879+74784C>T