ClinGen Allele Registry
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Canonical Allele Identifier:
CA15709691
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.69227030T>G
GRCh37
chr11:g.68994497T>G
Linked Data - Sequence & Population
gnomAD v2:
11:68994497 T / G
gnomAD v3:
11:69227030 T / G
gnomAD v4:
chr11-69227030-T-G
Joint Max Group AF
0.78354357 (AFR)
Genomes Max Group AF
0.78354357 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7931342
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.69227030T>G , CM000673.2:g.69227030T>G
GRCh38
NC_000011.9:g.68994497T>G , CM000673.1:g.68994497T>G
GRCh37
NC_000011.8:g.68751073T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'