ClinGen Allele Registry
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Canonical Allele Identifier:
CA14814273
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.33675156G>A
GRCh37
chr20:g.32262962G>A
Linked Data - Sequence & Population
gnomAD v2:
20:32262962 G / A
gnomAD v3:
20:33675156 G / A
gnomAD v4:
chr20-33675156-G-A
Joint Max Group AF
0.35585738 (EAS)
Genomes Max Group AF
0.35766886 (EAS)
Exomes Max Group AF
0.23544374 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3213183
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.33675156G>A , CM000682.2:g.33675156G>A
GRCh38
NC_000020.10:g.32262962G>A , CM000682.1:g.32262962G>A
GRCh37
NC_000020.9:g.31726623G>A
NCBI36
NG_046988.1:g.16249C>T
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