ClinGen Allele Registry
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Canonical Allele Identifier:
CA15651181
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99585609C>T
GRCh37
chr10:g.101345366C>T
Linked Data - Sequence & Population
gnomAD v2:
10:101345366 C / T
gnomAD v3:
10:99585609 C / T
gnomAD v4:
chr10-99585609-C-T
Joint Max Group AF
0.18719234 (NFE)
Genomes Max Group AF
0.18719234 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1035209
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99585609C>T , CM000672.2:g.99585609C>T
GRCh38
NC_000010.10:g.101345366C>T , CM000672.1:g.101345366C>T
GRCh37
NC_000010.9:g.101335356C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'