ClinGen Allele Registry
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Canonical Allele Identifier:
CA14857935
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.26344335C>T
GRCh37
chr21:g.27716654C>T
Linked Data - Sequence & Population
gnomAD v2:
21:27716654 C / T
gnomAD v3:
21:26344335 C / T
gnomAD v4:
chr21-26344335-C-T
Joint Max Group AF
0.76100134 (EAS)
Genomes Max Group AF
0.76100134 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9975851
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.26344335C>T , CM000683.2:g.26344335C>T
GRCh38
NC_000021.8:g.27716654C>T , CM000683.1:g.27716654C>T
GRCh37
NC_000021.7:g.26638525C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'