ClinGen Allele Registry
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Canonical Allele Identifier:
CA12249644
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.131907629A>C
GRCh37
chr6:g.132228769A>C
Linked Data - Sequence & Population
gnomAD v2:
6:132228769 A / C
gnomAD v3:
6:131907629 A / C
gnomAD v4:
chr6-131907629-A-C
Joint Max Group AF
0.30455547 (AFR)
Genomes Max Group AF
0.30457012 (AFR)
Exomes Max Group AF
0.17768 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6907728
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.131907629A>C , CM000668.2:g.131907629A>C
GRCh38
NC_000006.11:g.132228769A>C , CM000668.1:g.132228769A>C
GRCh37
NC_000006.10:g.132270462A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'