ClinGen Allele Registry
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Canonical Allele Identifier:
CA262321787
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr14:g.62265946T>C
GRCh37
chr14:g.62732664T>C
Linked Data - Sequence & Population
gnomAD v2:
14:62732664 T / C
gnomAD v3:
14:62265946 T / C
gnomAD v4:
chr14-62265946-T-C
Joint Max Group AF
0.38690795 (AFR)
Genomes Max Group AF
0.38690795 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10146615
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.62265946T>C , CM000676.2:g.62265946T>C
GRCh38
NC_000014.8:g.62732664T>C , CM000676.1:g.62732664T>C
GRCh37
NC_000014.7:g.61802417T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'