Canonical Allele Identifier: CA532693837
Gene: NRXN1-DT HGNC NCBI
dbSNP:
17868256
gnomAD v2:
2:52032773 A / C
gnomAD v3:
2:51805635 A / C
gnomAD v4:
chr2-51805635-A-C
Joint Max Group AF 0.00000488 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
MyVariant.info:
GRCh38 chr2:g.51805635A>C
GRCh37 chr2:g.52032773A>C
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Genomic Alleles

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

Transcript Alleles

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