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Canonical Allele Identifier:
CA13439645
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.27731216T>C
GRCh37
chr11:g.27752763T>C
Linked Data - Sequence & Population
gnomAD v2:
11:27752763 T / C
gnomAD v3:
11:27731216 T / C
gnomAD v4:
chr11-27731216-T-C
Joint Max Group AF
0.53816288 (NFE)
Genomes Max Group AF
0.53816288 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1491851
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.27731216T>C , CM000673.2:g.27731216T>C
GRCh38
NC_000011.9:g.27752763T>C , CM000673.1:g.27752763T>C
GRCh37
NC_000011.8:g.27709339T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'