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Canonical Allele Identifier:
CA317824452
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472718G>T
GRCh37
chr21:g.15845039G>T
Linked Data - Sequence & Population
gnomAD v2:
21:15845039 G / T
gnomAD v3:
21:14472718 G / T
gnomAD v4:
chr21-14472718-G-T
Joint Max Group AF
0.00016716 (AFR)
Genomes Max Group AF
0.00016716 (AFR)
Linked Data - NCBI & NCI
dbSNP:
185827062
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472718G>T , CM000683.2:g.14472718G>T
GRCh38
NC_000021.8:g.15845039G>T , CM000683.1:g.15845039G>T
GRCh37
NC_000021.7:g.14766910G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'