ClinGen Allele Registry
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Canonical Allele Identifier:
CA303851976
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.78897779C>T
GRCh37
chr18:g.76657779C>T
Linked Data - Sequence & Population
gnomAD v2:
18:76657779 C / T
gnomAD v3:
18:78897779 C / T
gnomAD v4:
chr18-78897779-C-T
Joint Max Group AF
0.34585508 (EAS)
Genomes Max Group AF
0.34585508 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9951602
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.78897779C>T , CM000680.2:g.78897779C>T
GRCh38
NC_000018.9:g.76657779C>T , CM000680.1:g.76657779C>T
GRCh37
NC_000018.8:g.74758767C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'