ClinGen Allele Registry
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Canonical Allele Identifier:
CA311066140
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.4188432G>A
GRCh37
chr20:g.4169079G>A
Linked Data - Sequence & Population
gnomAD v2:
20:4169079 G / A
gnomAD v3:
20:4188432 G / A
gnomAD v4:
chr20-4188432-G-A
Joint Max Group AF
0.17655422 (EAS)
Genomes Max Group AF
0.17655422 (EAS)
Linked Data - NCBI & NCI
dbSNP:
16989303
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.4188432G>A , CM000682.2:g.4188432G>A
GRCh38
NC_000020.10:g.4169079G>A , CM000682.1:g.4169079G>A
GRCh37
NC_000020.9:g.4117079G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'