ClinGen Allele Registry
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Canonical Allele Identifier:
CA14785693
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.23866372T>C
GRCh37
chr20:g.23847009T>C
Linked Data - Sequence & Population
gnomAD v2:
20:23847009 T / C
gnomAD v3:
20:23866372 T / C
gnomAD v4:
chr20-23866372-T-C
Joint Max Group AF
0.30438399 (EAS)
Genomes Max Group AF
0.30438399 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6138150
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.23866372T>C , CM000682.2:g.23866372T>C
GRCh38
NC_000020.10:g.23847009T>C , CM000682.1:g.23847009T>C
GRCh37
NC_000020.9:g.23795009T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'