ClinGen Allele Registry
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Canonical Allele Identifier:
CA13449703
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.114320294A>G
GRCh37
chr11:g.114191016A>G
Linked Data - Sequence & Population
gnomAD v2:
11:114191016 A / G
gnomAD v3:
11:114320294 A / G
gnomAD v4:
chr11-114320294-A-G
Joint Max Group AF
0.72086411 (AFR)
Genomes Max Group AF
0.72086411 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2847476
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.114320294A>G , CM000673.2:g.114320294A>G
GRCh38
NC_000011.9:g.114191016A>G , CM000673.1:g.114191016A>G
GRCh37
NC_000011.8:g.113696226A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'