ClinGen Allele Registry
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Canonical Allele Identifier:
CA13647865
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.56045425A>G
GRCh37
chr12:g.56439209A>G
Linked Data - Sequence & Population
gnomAD v2:
12:56439209 A / G
gnomAD v3:
12:56045425 A / G
gnomAD v4:
chr12-56045425-A-G
Joint Max Group AF
0.32260647 (SAS)
Genomes Max Group AF
0.32260647 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12580100
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.56045425A>G , CM000674.2:g.56045425A>G
GRCh38
NC_000012.11:g.56439209A>G , CM000674.1:g.56439209A>G
GRCh37
NC_000012.10:g.54725476A>G
NCBI36
NG_023201.1:g.8524A>G
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