ClinGen Allele Registry
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Canonical Allele Identifier:
CA11925786
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.33985752T>C
GRCh37
chr5:g.33985857T>C
Linked Data - Sequence & Population
gnomAD v2:
5:33985857 T / C
gnomAD v3:
5:33985752 T / C
gnomAD v4:
chr5-33985752-T-C
Joint Max Group AF
0.82634572 (EAS)
Genomes Max Group AF
0.82634572 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6867641
2126596605
2126596623
2126596643
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.33985752T>C , CM000667.2:g.33985752T>C
GRCh38
NC_000005.9:g.33985857T>C , CM000667.1:g.33985857T>C
GRCh37
NC_000005.8:g.34021614T>C
NCBI36
NG_011691.2:g.3924A>G
NG_016211.1:g.27364A>G
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