Allele Registry

Canonical Allele Identifier: CA11151995

Gene: NRXN1-DT HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.51710713A>G

GRCh37 chr2:g.51937851A>G

Linked Data - Sequence & Population

gnomAD v2:

2:51937851 A / G

gnomAD v3:

2:51710713 A / G

gnomAD v4:

chr2-51710713-A-G

Joint Max Group AF 0.85231252 (SAS)

Genomes Max Group AF 0.85231252 (SAS)

Linked Data - NCBI & NCI

dbSNP:

2063871

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.51710713A>G , CM000664.2:g.51710713A>G	GRCh38
NC_000002.11:g.51937851A>G , CM000664.1:g.51937851A>G	GRCh37
NC_000002.10:g.51791355A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245003.1:n.754-51376A>G
NR_135237.1:n.754-51376A>G

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