ClinGen Allele Registry
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Canonical Allele Identifier:
CA251475943
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.63060217G>T
Linked Data - Sequence & Population
gnomAD v3:
13:63060217 G / T
gnomAD v4:
chr13-63060217-G-T
Joint Max Group AF
0.06862795 (NFE)
Genomes Max Group AF
0.06862795 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9317284
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.63060217G>T , CM000675.2:g.63060217G>T
GRCh38
Search 100 bp 5'
Search 100 bp 3'