Canonical Allele Identifier: CA48253093

Gene: NRXN1-DT

Linked Data

• dbSNP Id: rs915721866
• gnomAD v2: 2-52072553-G-C
• gnomAD v3: 2-51845415-G-C
• gnomAD v4: 2-51845415-G-C
• MyVariant Identifiers: chr2:g.52072553G>C (hg19) ; chr2:g.51845415G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51845415G>C , CM000664.2:g.51845415G>C	GRCh38
NC_000002.11:g.52072553G>C , CM000664.1:g.52072553G>C	GRCh37
NC_000002.10:g.51926057G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.840-16034G>C
NR_135237.1:n.840-16034G>C