ClinGen Allele Registry
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Canonical Allele Identifier:
CA15798242
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.53393956T>C
GRCh37
chr13:g.53968091T>C
Linked Data - Sequence & Population
gnomAD v2:
13:53968091 T / C
gnomAD v3:
13:53393956 T / C
gnomAD v4:
chr13-53393956-T-C
Joint Max Group AF
0.16110023 (AFR)
Genomes Max Group AF
0.16110023 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10507577
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.53393956T>C , CM000675.2:g.53393956T>C
GRCh38
NC_000013.10:g.53968091T>C , CM000675.1:g.53968091T>C
GRCh37
NC_000013.9:g.52866092T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'