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Canonical Allele Identifier:
CA15692683
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.118274971C>T
GRCh37
chr11:g.118145686C>T
Linked Data - Sequence & Population
gnomAD v2:
11:118145686 C / T
gnomAD v3:
11:118274971 C / T
gnomAD v4:
chr11-118274971-C-T
Joint Max Group AF
0.51239703 (EAS)
Genomes Max Group AF
0.51239703 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17122021
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.118274971C>T , CM000673.2:g.118274971C>T
GRCh38
NC_000011.9:g.118145686C>T , CM000673.1:g.118145686C>T
GRCh37
NC_000011.8:g.117650896C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'