ClinGen Allele Registry
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Canonical Allele Identifier:
CA13686589
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.43318486G>A
GRCh37
chr12:g.43712289G>A
Linked Data - Sequence & Population
gnomAD v2:
12:43712289 G / A
gnomAD v3:
12:43318486 G / A
gnomAD v4:
chr12-43318486-G-A
Joint Max Group AF
0.9742134 (EAS)
Genomes Max Group AF
0.9742134 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1027615
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.43318486G>A , CM000674.2:g.43318486G>A
GRCh38
NC_000012.11:g.43712289G>A , CM000674.1:g.43712289G>A
GRCh37
NC_000012.10:g.41998556G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'