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Canonical Allele Identifier:
CA172969823
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.17472318C>T
GRCh37
chr8:g.17329827C>T
Linked Data - Sequence & Population
gnomAD v2:
8:17329827 C / T
gnomAD v3:
8:17472318 C / T
gnomAD v4:
chr8-17472318-C-T
Joint Max Group AF
0.99068247 (NFE)
Genomes Max Group AF
0.99068247 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2720508
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.17472318C>T , CM000670.2:g.17472318C>T
GRCh38
NC_000008.10:g.17329827C>T , CM000670.1:g.17329827C>T
GRCh37
Search 100 bp 5'
Search 100 bp 3'