Canonical Allele Identifier: CA532694359

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs1032792458
• gnomAD v2: 2-52072564-G-T
• MyVariant Identifiers: chr2:g.52072564G>T (hg19) ; chr2:g.51845426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845426G>T , CM000664.2:g.51845426G>T	GRCh38
NC_000002.11:g.52072564G>T , CM000664.1:g.52072564G>T	GRCh37
NC_000002.10:g.51926068G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16023G>T
NR_135237.1:n.840-16023G>T