ClinGen Allele Registry
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Canonical Allele Identifier:
CA15768950
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.120951159A>C
GRCh37
chr12:g.121388962A>C
Linked Data - Sequence & Population
gnomAD v2:
12:121388962 A / C
gnomAD v3:
12:120951159 A / C
gnomAD v4:
chr12-120951159-A-C
Joint Max Group AF
0.8708738 (AFR)
Genomes Max Group AF
0.8708738 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2650000
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.120951159A>C , CM000674.2:g.120951159A>C
GRCh38
NC_000012.11:g.121388962A>C , CM000674.1:g.121388962A>C
GRCh37
NC_000012.10:g.119873345A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'