ClinGen Allele Registry
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Canonical Allele Identifier:
CA138929428
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.52186311G>A
GRCh37
chr6:g.52051109G>A
Linked Data - Sequence & Population
gnomAD v2:
6:52051109 G / A
gnomAD v3:
6:52186311 G / A
gnomAD v4:
chr6-52186311-G-A
Joint Max Group AF
0.10945332 (EAS)
Genomes Max Group AF
0.09697967 (EAS)
Exomes Max Group AF
0.11039886 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8193037
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.52186311G>A , CM000668.2:g.52186311G>A
GRCh38
NC_000006.11:g.52051109G>A , CM000668.1:g.52051109G>A
GRCh37
NC_000006.10:g.52159068G>A
NCBI36
NG_033021.1:g.4925G>A
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