ClinGen Allele Registry
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Canonical Allele Identifier:
CA14763610
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.60693652G>A
GRCh37
chr20:g.59268710G>A
Linked Data - Sequence & Population
gnomAD v2:
20:59268710 G / A
gnomAD v3:
20:60693652 G / A
gnomAD v4:
chr20-60693652-G-A
Joint Max Group AF
0.41384877 (SAS)
Genomes Max Group AF
0.41384877 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6027755
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.60693652G>A , CM000682.2:g.60693652G>A
GRCh38
NC_000020.10:g.59268710G>A , CM000682.1:g.59268710G>A
GRCh37
NC_000020.9:g.58702105G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'