ClinGen Allele Registry
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Canonical Allele Identifier:
CA15710259
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.36480237A>T
GRCh37
chr11:g.36501787A>T
Linked Data - Sequence & Population
gnomAD v2:
11:36501787 A / T
gnomAD v3:
11:36480237 A / T
gnomAD v4:
chr11-36480237-A-T
Joint Max Group AF
0.91772352 (EAS)
Genomes Max Group AF
0.91772352 (EAS)
Linked Data - NCBI & NCI
dbSNP:
331463
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.36480237A>T , CM000673.2:g.36480237A>T
GRCh38
NC_000011.9:g.36501787A>T , CM000673.1:g.36501787A>T
GRCh37
NC_000011.8:g.36458363A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'