ClinGen Allele Registry
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Canonical Allele Identifier:
CA14399072
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.29348208C>T
GRCh37
chr17:g.27675226C>T
Linked Data - Sequence & Population
gnomAD v2:
17:27675226 C / T
gnomAD v3:
17:29348208 C / T
gnomAD v4:
chr17-29348208-C-T
Joint Max Group AF
0.86359573 (EAS)
Genomes Max Group AF
0.86359573 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11653144
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.29348208C>T , CM000679.2:g.29348208C>T
GRCh38
NC_000017.10:g.27675226C>T , CM000679.1:g.27675226C>T
GRCh37
NC_000017.9:g.24699352C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'