ClinGen Allele Registry
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Canonical Allele Identifier:
CA15654498
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117586327G>A
GRCh37
chr10:g.119345838G>A
Linked Data - Sequence & Population
gnomAD v2:
10:119345838 G / A
gnomAD v3:
10:117586327 G / A
gnomAD v4:
chr10-117586327-G-A
Joint Max Group AF
0.24965822 (AFR)
Genomes Max Group AF
0.24965822 (AFR)
Linked Data - NCBI & NCI
dbSNP:
181601
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117586327G>A , CM000672.2:g.117586327G>A
GRCh38
NC_000010.10:g.119345838G>A , CM000672.1:g.119345838G>A
GRCh37
NC_000010.9:g.119335828G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'