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Canonical Allele Identifier:
CA13791653
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.64376290T>C
GRCh37
chr13:g.64950422T>C
Linked Data - Sequence & Population
gnomAD v2:
13:64950422 T / C
gnomAD v3:
13:64376290 T / C
gnomAD v4:
chr13-64376290-T-C
Joint Max Group AF
0.51185741 (AMR)
Genomes Max Group AF
0.51185741 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1340319
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.64376290T>C , CM000675.2:g.64376290T>C
GRCh38
NC_000013.10:g.64950422T>C , CM000675.1:g.64950422T>C
GRCh37
NC_000013.9:g.63848423T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'