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Canonical Allele Identifier:
CA15749121
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.43315125C>G
GRCh37
chr12:g.43708928C>G
Linked Data - Sequence & Population
gnomAD v2:
12:43708928 C / G
gnomAD v3:
12:43315125 C / G
gnomAD v4:
chr12-43315125-C-G
Joint Max Group AF
0.9742134 (EAS)
Genomes Max Group AF
0.9742134 (EAS)
Linked Data - NCBI & NCI
dbSNP:
905080
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.43315125C>G , CM000674.2:g.43315125C>G
GRCh38
NC_000012.11:g.43708928C>G , CM000674.1:g.43708928C>G
GRCh37
NC_000012.10:g.41995195C>G
NCBI36
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