ClinGen Allele Registry
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Canonical Allele Identifier:
CA13870902
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.69033320C>T
GRCh37
chr13:g.69607452C>T
Linked Data - Sequence & Population
gnomAD v2:
13:69607452 C / T
gnomAD v3:
13:69033320 C / T
gnomAD v4:
chr13-69033320-C-T
Joint Max Group AF
0.31780879 (SAS)
Genomes Max Group AF
0.31780879 (SAS)
Linked Data - NCBI & NCI
dbSNP:
9529500
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.69033320C>T , CM000675.2:g.69033320C>T
GRCh38
NC_000013.10:g.69607452C>T , CM000675.1:g.69607452C>T
GRCh37
NC_000013.9:g.68505453C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'