ClinGen Allele Registry
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Canonical Allele Identifier:
CA13394718
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102519261A>G
GRCh37
chr11:g.102389992A>G
Linked Data - Sequence & Population
gnomAD v2:
11:102389992 A / G
gnomAD v3:
11:102519261 A / G
gnomAD v4:
chr11-102519261-A-G
Joint Max Group AF
0.26749605 (EAS)
Genomes Max Group AF
0.26749605 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10895304
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102519261A>G , CM000673.2:g.102519261A>G
GRCh38
NC_000011.9:g.102389992A>G , CM000673.1:g.102389992A>G
GRCh37
NC_000011.8:g.101895202A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'