ClinGen Allele Registry
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Canonical Allele Identifier:
CA14779824
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.57416639G>A
GRCh37
chr20:g.55991695G>A
Linked Data - Sequence & Population
gnomAD v2:
20:55991695 G / A
gnomAD v3:
20:57416639 G / A
gnomAD v4:
chr20-57416639-G-A
Joint Max Group AF
0.49078319 (EAS)
Genomes Max Group AF
0.49078319 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6092477
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.57416639G>A , CM000682.2:g.57416639G>A
GRCh38
NC_000020.10:g.55991695G>A , CM000682.1:g.55991695G>A
GRCh37
NC_000020.9:g.55425101G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'