ClinGen Allele Registry
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Canonical Allele Identifier:
CA14836093
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.52940622G>A
GRCh37
chr20:g.51557161G>A
Linked Data - Sequence & Population
gnomAD v2:
20:51557161 G / A
gnomAD v3:
20:52940622 G / A
gnomAD v4:
chr20-52940622-G-A
Joint Max Group AF
0.51296285 (EAS)
Genomes Max Group AF
0.51296285 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6097169
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.52940622G>A , CM000682.2:g.52940622G>A
GRCh38
NC_000020.10:g.51557161G>A , CM000682.1:g.51557161G>A
GRCh37
NC_000020.9:g.50990568G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'