ClinGen Allele Registry
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Canonical Allele Identifier:
CA13979272
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.65821192C>T
GRCh37
chr14:g.66287910C>T
Linked Data - Sequence & Population
gnomAD v2:
14:66287910 C / T
gnomAD v3:
14:65821192 C / T
gnomAD v4:
chr14-65821192-C-T
Joint Max Group AF
0.93103409 (EAS)
Genomes Max Group AF
0.93103409 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7494064
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.65821192C>T , CM000676.2:g.65821192C>T
GRCh38
NC_000014.8:g.66287910C>T , CM000676.1:g.66287910C>T
GRCh37
NC_000014.7:g.65357663C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'