ClinGen Allele Registry
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Canonical Allele Identifier:
CA14889985
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr21:g.23770802G>A
GRCh37
chr21:g.25143119G>A
Linked Data - Sequence & Population
gnomAD v2:
21:25143119 G / A
gnomAD v3:
21:23770802 G / A
gnomAD v4:
chr21-23770802-G-A
Joint Max Group AF
0.84150453 (EAS)
Genomes Max Group AF
0.84150453 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2828520
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.23770802G>A , CM000683.2:g.23770802G>A
GRCh38
NC_000021.8:g.25143119G>A , CM000683.1:g.25143119G>A
GRCh37
NC_000021.7:g.24064990G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'