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Canonical Allele Identifier:
CA12188529
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32689801T>C
GRCh37
chr6:g.32657578T>C
Linked Data - Sequence & Population
gnomAD v2:
6:32657578 T / C
gnomAD v3:
6:32689801 T / C
gnomAD v4:
chr6-32689801-T-C
Joint Max Group AF
0.50236189 (SAS)
Genomes Max Group AF
0.50236189 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7774434
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32689801T>C , CM000668.2:g.32689801T>C
GRCh38
NC_000006.11:g.32657578T>C , CM000668.1:g.32657578T>C
GRCh37
NC_000006.10:g.32765556T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'