ClinGen Allele Registry
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Canonical Allele Identifier:
CA591903116
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.18139486C>G
GRCh37
chr10:g.18428415C>G
Linked Data - Sequence & Population
gnomAD v2:
10:18428415 C / G
gnomAD v3:
10:18139486 C / G
gnomAD v4:
chr10-18139486-C-G
Joint Max Group AF
0.00032016 (AFR)
Genomes Max Group AF
0.00032016 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10764319
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.18139486C>G , CM000672.2:g.18139486C>G
GRCh38
NC_000010.10:g.18428415C>G , CM000672.1:g.18428415C>G
GRCh37
NC_000010.9:g.18468421C>G
NCBI36
NG_016195.1:g.3810C>G
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