ClinGen Allele Registry
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Canonical Allele Identifier:
CA13562001
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.91151171A>C
GRCh37
chr11:g.90884339A>C
Linked Data - Sequence & Population
gnomAD v2:
11:90884339 A / C
gnomAD v3:
11:91151171 A / C
gnomAD v4:
chr11-91151171-A-C
Joint Max Group AF
0.79170666 (SAS)
Genomes Max Group AF
0.79170666 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1528753
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.91151171A>C , CM000673.2:g.91151171A>C
GRCh38
NC_000011.9:g.90884339A>C , CM000673.1:g.90884339A>C
GRCh37
NC_000011.8:g.90523987A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'