Canonical Allele Identifier: CA48247613
Gene: NRXN1-DT HGNC NCBI
dbSNP:
17868256
gnomAD v2:
2:52032773 A / G
gnomAD v3:
2:51805635 A / G
gnomAD v4:
chr2-51805635-A-G
Joint Max Group AF 0.48620501 (EAS)
Genomes Max Group AF 0.48620501 (EAS)
MyVariant.info:
GRCh38 chr2:g.51805635A>G
GRCh37 chr2:g.52032773A>G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51805635A>G , CM000664.2:g.51805635A>G GRCh38
NC_000002.11:g.52032773A>G , CM000664.1:g.52032773A>G GRCh37
NC_000002.10:g.51886277A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.839+43461A>G
NR_135237.1:n.839+43461A>G
Search 100 bp 5'
Search 100 bp 3'