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Canonical Allele Identifier:
CA13446934
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.93473731C>G
GRCh37
chr11:g.93206897C>G
Linked Data - Sequence & Population
gnomAD v2:
11:93206897 C / G
gnomAD v3:
11:93473731 C / G
gnomAD v4:
chr11-93473731-C-G
Joint Max Group AF
0.70307498 (EAS)
Genomes Max Group AF
0.70307498 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2605593
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.93473731C>G , CM000673.2:g.93473731C>G
GRCh38
NC_000011.9:g.93206897C>G , CM000673.1:g.93206897C>G
GRCh37
NC_000011.8:g.92846545C>G
NCBI36
Search 100 bp 5'
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