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Canonical Allele Identifier:
CA241234298
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.91112088del
GRCh37
chr12:g.91505865del
Linked Data - Sequence & Population
gnomAD v2:
12:91505864 CT / C
gnomAD v3:
12:91112087 CT / C
gnomAD v4:
chr12-91112087-CT-C
Joint Max Group AF
0.24963944 (EAS)
Genomes Max Group AF
0.24963944 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17018757
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91112088del , CM000674.2:g.91112088del
GRCh38
NC_000012.11:g.91505865del , CM000674.1:g.91505865del
GRCh37
NC_000012.10:g.90029996del
NCBI36
Search 100 bp 5'
Search 100 bp 3'