ClinGen Allele Registry
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Canonical Allele Identifier:
CA13590093
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.56007301G>A
GRCh37
chr12:g.56401085G>A
Linked Data - Sequence & Population
gnomAD v2:
12:56401085 G / A
gnomAD v3:
12:56007301 G / A
gnomAD v4:
chr12-56007301-G-A
Joint Max Group AF
0.75936706 (EAS)
Genomes Max Group AF
0.75936706 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10876864
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.56007301G>A , CM000674.2:g.56007301G>A
GRCh38
NC_000012.11:g.56401085G>A , CM000674.1:g.56401085G>A
GRCh37
NC_000012.10:g.54687352G>A
NCBI36
NG_008136.1:g.15043G>A
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