ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14910631
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr21:g.39097594A>G
GRCh37
chr21:g.40469520A>G
Linked Data - Sequence & Population
gnomAD v2:
21:40469520 A / G
gnomAD v3:
21:39097594 A / G
gnomAD v4:
chr21-39097594-A-G
Joint Max Group AF
0.48520831 (NFE)
Genomes Max Group AF
0.48520831 (NFE)
Linked Data - NCBI & NCI
dbSNP:
378108
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.39097594A>G , CM000683.2:g.39097594A>G
GRCh38
NC_000021.8:g.40469520A>G , CM000683.1:g.40469520A>G
GRCh37
NC_000021.7:g.39391390A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'