ClinGen Allele Registry
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Canonical Allele Identifier:
CA15734169
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.69187442C>A
GRCh37
chr12:g.69581222C>A
Linked Data - Sequence & Population
gnomAD v2:
12:69581222 C / A
gnomAD v3:
12:69187442 C / A
gnomAD v4:
chr12-69187442-C-A
Joint Max Group AF
0.17906703 (SAS)
Genomes Max Group AF
0.17906703 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12367448
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.69187442C>A , CM000674.2:g.69187442C>A
GRCh38
NC_000012.11:g.69581222C>A , CM000674.1:g.69581222C>A
GRCh37
NC_000012.10:g.67867489C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'