ClinGen Allele Registry
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Canonical Allele Identifier:
CA13519097
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.45062980A>G
GRCh37
chr11:g.45084531A>G
Linked Data - Sequence & Population
gnomAD v2:
11:45084531 A / G
gnomAD v3:
11:45062980 A / G
gnomAD v4:
chr11-45062980-A-G
Joint Max Group AF
0.51405133 (AFR)
Genomes Max Group AF
0.51405133 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7951911
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.45062980A>G , CM000673.2:g.45062980A>G
GRCh38
NC_000011.9:g.45084531A>G , CM000673.1:g.45084531A>G
GRCh37
NC_000011.8:g.45041107A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'