ClinGen Allele Registry
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Canonical Allele Identifier:
CA11489066
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186622052G>C
GRCh37
chr3:g.186339841G>C
Linked Data - Sequence & Population
gnomAD v2:
3:186339841 G / C
gnomAD v3:
3:186622052 G / C
gnomAD v4:
chr3-186622052-G-C
Joint Max Group AF
0.33698341 (AFR)
Genomes Max Group AF
0.33698341 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6787344
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186622052G>C , CM000665.2:g.186622052G>C
GRCh38
NC_000003.11:g.186339841G>C , CM000665.1:g.186339841G>C
GRCh37
NC_000003.10:g.187822535G>C
NCBI36
NG_011436.1:g.13992G>C
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