ClinGen Allele Registry
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Canonical Allele Identifier:
CA14868726
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.27362678C>T
GRCh37
chr21:g.28734997C>T
Linked Data - Sequence & Population
gnomAD v2:
21:28734997 C / T
gnomAD v3:
21:27362678 C / T
gnomAD v4:
chr21-27362678-C-T
Joint Max Group AF
0.60314699 (NFE)
Genomes Max Group AF
0.60314699 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9977499
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.27362678C>T , CM000683.2:g.27362678C>T
GRCh38
NC_000021.8:g.28734997C>T , CM000683.1:g.28734997C>T
GRCh37
NC_000021.7:g.27656868C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'