ClinGen Allele Registry
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Canonical Allele Identifier:
CA12231451
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32184665A>G
GRCh37
chr6:g.32152442A>G
Linked Data - Sequence & Population
gnomAD v2:
6:32152442 A / G
gnomAD v3:
6:32184665 A / G
gnomAD v4:
chr6-32184665-A-G
Joint Max Group AF
0.17400071 (NFE)
Genomes Max Group AF
0.17762008 (NFE)
Exomes Max Group AF
0.16520743 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1800625
2113351122
2113351141
2113351156
2113351207
2113351232
2113351249
2113351271
2113351295
2113351314
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32184665A>G , CM000668.2:g.32184665A>G
GRCh38
NC_000006.11:g.32152442A>G , CM000668.1:g.32152442A>G
GRCh37
NC_000006.10:g.32260420A>G
NCBI36
NG_029868.1:g.4658T>C
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