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Canonical Allele Identifier:
CA15763925
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.116889787T>C
GRCh37
chr12:g.117327592T>C
Linked Data - Sequence & Population
gnomAD v2:
12:117327592 T / C
gnomAD v3:
12:116889787 T / C
gnomAD v4:
chr12-116889787-T-C
Joint Max Group AF
0.37315762 (AFR)
Genomes Max Group AF
0.37315762 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7294919
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.116889787T>C , CM000674.2:g.116889787T>C
GRCh38
NC_000012.11:g.117327592T>C , CM000674.1:g.117327592T>C
GRCh37
NC_000012.10:g.115811975T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'