ClinGen Allele Registry
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Canonical Allele Identifier:
CA13861833
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.68665820A>G
GRCh37
chr13:g.69239952A>G
Linked Data - Sequence & Population
gnomAD v2:
13:69239952 A / G
gnomAD v3:
13:68665820 A / G
gnomAD v4:
chr13-68665820-A-G
Joint Max Group AF
0.66851244 (EAS)
Genomes Max Group AF
0.66851244 (EAS)
Linked Data - NCBI & NCI
dbSNP:
287354
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.68665820A>G , CM000675.2:g.68665820A>G
GRCh38
NC_000013.10:g.69239952A>G , CM000675.1:g.69239952A>G
GRCh37
NC_000013.9:g.68137953A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'