ClinGen Allele Registry
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Canonical Allele Identifier:
CA13648936
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.66187836G>A
GRCh37
chr12:g.66581616G>A
Linked Data - Sequence & Population
gnomAD v2:
12:66581616 G / A
gnomAD v3:
12:66187836 G / A
gnomAD v4:
chr12-66187836-G-A
Joint Max Group AF
0.86269304 (EAS)
Genomes Max Group AF
0.86269304 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1732887
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.66187836G>A , CM000674.2:g.66187836G>A
GRCh38
NC_000012.11:g.66581616G>A , CM000674.1:g.66581616G>A
GRCh37
NC_000012.10:g.64867883G>A
NCBI36
NG_021194.1:g.3639G>A
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