ClinGen Allele Registry
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Canonical Allele Identifier:
CA14095952
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.28760947C>T
GRCh37
chr15:g.29006093C>T
Linked Data - Sequence & Population
gnomAD v2:
15:29006093 C / T
gnomAD v3:
15:28760947 C / T
gnomAD v4:
chr15-28760947-C-T
Joint Max Group AF
0.435985 (NFE)
Genomes Max Group AF
0.435985 (NFE)
Linked Data - NCBI & NCI
dbSNP:
8033165
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.28760947C>T , CM000677.2:g.28760947C>T
GRCh38
NC_000015.9:g.29006093C>T , CM000677.1:g.29006093C>T
GRCh37
NC_000015.8:g.26805134C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'