ClinGen Allele Registry
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Canonical Allele Identifier:
CA16449074
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.74660813A>G
GRCh37
chr12:g.75054593A>G
Linked Data - Sequence & Population
gnomAD v2:
12:75054593 A / G
gnomAD v3:
12:74660813 A / G
gnomAD v4:
chr12-74660813-A-G
Joint Max Group AF
0.72908614 (AFR)
Genomes Max Group AF
0.72908614 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7311660
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.74660813A>G , CM000674.2:g.74660813A>G
GRCh38
NC_000012.11:g.75054593A>G , CM000674.1:g.75054593A>G
GRCh37
NC_000012.10:g.73340860A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'