ClinGen Allele Registry
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Canonical Allele Identifier:
CA12859634
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.27480274A>C
GRCh37
chr8:g.27337791A>C
Linked Data - Sequence & Population
gnomAD v2:
8:27337791 A / C
gnomAD v3:
8:27480274 A / C
gnomAD v4:
chr8-27480274-A-C
Joint Max Group AF
0.68632174 (AFR)
Genomes Max Group AF
0.68632174 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2741335
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.27480274A>C , CM000670.2:g.27480274A>C
GRCh38
NC_000008.10:g.27337791A>C , CM000670.1:g.27337791A>C
GRCh37
NC_000008.9:g.27393708A>C
NCBI36
NG_015827.1:g.4023T>G
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