ClinGen Allele Registry
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Canonical Allele Identifier:
CA211444631
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.87852267T>C
GRCh37
chr10:g.89612024T>C
Linked Data - Sequence & Population
gnomAD v2:
10:89612024 T / C
gnomAD v3:
10:87852267 T / C
gnomAD v4:
chr10-87852267-T-C
Joint Max Group AF
0.34069696 (EAS)
Genomes Max Group AF
0.34069696 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11202586
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.87852267T>C , CM000672.2:g.87852267T>C
GRCh38
NC_000010.10:g.89612024T>C , CM000672.1:g.89612024T>C
GRCh37
NC_000010.9:g.89602004T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'