ClinGen Allele Registry
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Canonical Allele Identifier:
CA13977778
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.55079608T>C
GRCh37
chr14:g.55546326T>C
Linked Data - Sequence & Population
gnomAD v2:
14:55546326 T / C
gnomAD v3:
14:55079608 T / C
gnomAD v4:
chr14-55079608-T-C
Joint Max Group AF
0.67011065 (AFR)
Genomes Max Group AF
0.67011065 (AFR)
Linked Data - NCBI & NCI
dbSNP:
873061
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.55079608T>C , CM000676.2:g.55079608T>C
GRCh38
NC_000014.8:g.55546326T>C , CM000676.1:g.55546326T>C
GRCh37
NC_000014.7:g.54616079T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'