ClinGen Allele Registry
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Canonical Allele Identifier:
CA15751125
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.109095724T>C
GRCh37
chr12:g.109533529T>C
Linked Data - Sequence & Population
gnomAD v2:
12:109533529 T / C
gnomAD v3:
12:109095724 T / C
gnomAD v4:
chr12-109095724-T-C
Joint Max Group AF
0.30825244 (EAS)
Genomes Max Group AF
0.30825244 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3890995
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.109095724T>C , CM000674.2:g.109095724T>C
GRCh38
NC_000012.11:g.109533529T>C , CM000674.1:g.109533529T>C
GRCh37
NC_000012.10:g.108017912T>C
NCBI36
NG_007284.1:g.3115T>C , LRG_124:g.3115T>C
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