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Canonical Allele Identifier:
CA15633514
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117989592T>C
GRCh37
chr10:g.119749103T>C
Linked Data - Sequence & Population
gnomAD v2:
10:119749103 T / C
gnomAD v3:
10:117989592 T / C
gnomAD v4:
chr10-117989592-T-C
Joint Max Group AF
0.59575115 (NFE)
Genomes Max Group AF
0.59575115 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12218935
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117989592T>C , CM000672.2:g.117989592T>C
GRCh38
NC_000010.10:g.119749103T>C , CM000672.1:g.119749103T>C
GRCh37
NC_000010.9:g.119739093T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'