ClinGen Allele Registry
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Canonical Allele Identifier:
CA16396999
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.86368524A>G
GRCh37
chr10:g.88128281A>G
Linked Data - Sequence & Population
gnomAD v2:
10:88128281 A / G
gnomAD v3:
10:86368524 A / G
gnomAD v4:
chr10-86368524-A-G
Joint Max Group AF
0.81679315 (AFR)
Genomes Max Group AF
0.81679315 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3814614
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.86368524A>G , CM000672.2:g.86368524A>G
GRCh38
NC_000010.10:g.88128281A>G , CM000672.1:g.88128281A>G
GRCh37
NC_000010.9:g.88118261A>G
NCBI36
NG_011875.1:g.2970T>C
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