Canonical Allele Identifier: CA48253058

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs551980940
• MyVariant Identifiers: chr2:g.51845191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845191C>T , CM000664.2:g.51845191C>T	GRCh38
NC_000002.11:g.52072329C>T , CM000664.1:g.52072329C>T	GRCh37
NC_000002.10:g.51925833C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245003.1:n.840-16258C>T
NR_135237.1:n.840-16258C>T