ClinGen Allele Registry
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Canonical Allele Identifier:
CA136964099
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32432567C>A
GRCh37
chr6:g.32400344C>A
Linked Data - Sequence & Population
gnomAD v2:
6:32400344 C / A
gnomAD v3:
6:32432567 C / A
gnomAD v4:
chr6-32432567-C-A
Joint Max Group AF
0.28859128 (AFR)
Genomes Max Group AF
0.28859128 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9501626
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32432567C>A , CM000668.2:g.32432567C>A
GRCh38
NC_000006.11:g.32400344C>A , CM000668.1:g.32400344C>A
GRCh37
NC_000006.10:g.32508322C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'