ClinGen Allele Registry
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Canonical Allele Identifier:
CA225335619
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.86076782C>T
GRCh37
chr11:g.85787824C>T
Linked Data - Sequence & Population
gnomAD v2:
11:85787824 C / T
gnomAD v3:
11:86076782 C / T
gnomAD v4:
chr11-86076782-C-T
Joint Max Group AF
0.86106213 (AFR)
Genomes Max Group AF
0.86106213 (AFR)
Linked Data - NCBI & NCI
dbSNP:
536841
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.86076782C>T , CM000673.2:g.86076782C>T
GRCh38
NC_000011.9:g.85787824C>T , CM000673.1:g.85787824C>T
GRCh37
NC_000011.8:g.85465472C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'