ClinGen Allele Registry
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Canonical Allele Identifier:
CA89665028
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186838248T>C
GRCh37
chr3:g.186556037T>C
Linked Data - Sequence & Population
gnomAD v2:
3:186556037 T / C
gnomAD v3:
3:186838248 T / C
gnomAD v4:
chr3-186838248-T-C
Joint Max Group AF
0.31556899 (AFR)
Genomes Max Group AF
0.31556899 (AFR)
Linked Data - NCBI & NCI
dbSNP:
822387
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186838248T>C , CM000665.2:g.186838248T>C
GRCh38
NC_000003.11:g.186556037T>C , CM000665.1:g.186556037T>C
GRCh37
NC_000003.10:g.188038731T>C
NCBI36
NG_021140.1:g.575T>C
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