ClinGen Allele Registry
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Canonical Allele Identifier:
CA14798316
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.40399796C>A
GRCh37
chr20:g.39028436C>A
Linked Data - Sequence & Population
gnomAD v2:
20:39028436 C / A
gnomAD v3:
20:40399796 C / A
gnomAD v4:
chr20-40399796-C-A
Joint Max Group AF
0.24914575 (AFR)
Genomes Max Group AF
0.24914575 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8124695
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.40399796C>A , CM000682.2:g.40399796C>A
GRCh38
NC_000020.10:g.39028436C>A , CM000682.1:g.39028436C>A
GRCh37
NC_000020.9:g.38461850C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'