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Canonical Allele Identifier:
CA15816979
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.53962637C>T
GRCh37
chr14:g.54429355C>T
Linked Data - Sequence & Population
gnomAD v2:
14:54429355 C / T
gnomAD v3:
14:53962637 C / T
gnomAD v4:
chr14-53962637-C-T
Joint Max Group AF
0.84404002 (EAS)
Genomes Max Group AF
0.84404002 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1957860
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.53962637C>T , CM000676.2:g.53962637C>T
GRCh38
NC_000014.8:g.54429355C>T , CM000676.1:g.54429355C>T
GRCh37
NC_000014.7:g.53499105C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'