ClinGen Allele Registry
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Canonical Allele Identifier:
CA10576171
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.69430244C>T
GRCh37
chr12:g.69824024C>T
Linked Data - Sequence & Population
gnomAD v2:
12:69824024 C / T
gnomAD v3:
12:69430244 C / T
gnomAD v4:
chr12-69430244-C-T
Joint Max Group AF
0.29849557 (AFR)
Genomes Max Group AF
0.29849557 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7297610
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.69430244C>T , CM000674.2:g.69430244C>T
GRCh38
NC_000012.11:g.69824024C>T , CM000674.1:g.69824024C>T
GRCh37
NC_000012.10:g.68110291C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'