ClinGen Allele Registry
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Canonical Allele Identifier:
CA14827933
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.21872462C>T
GRCh37
chr20:g.21853100C>T
Linked Data - Sequence & Population
gnomAD v2:
20:21853100 C / T
gnomAD v3:
20:21872462 C / T
gnomAD v4:
chr20-21872462-C-T
Joint Max Group AF
0.58499869 (AFR)
Genomes Max Group AF
0.58499869 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2180439
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.21872462C>T , CM000682.2:g.21872462C>T
GRCh38
NC_000020.10:g.21853100C>T , CM000682.1:g.21853100C>T
GRCh37
NC_000020.9:g.21801100C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'