ClinGen Allele Registry
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Canonical Allele Identifier:
CA16326332
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.11486171A>G
GRCh37
chr8:g.11343680A>G
Linked Data - Sequence & Population
gnomAD v2:
8:11343680 A / G
gnomAD v3:
8:11486171 A / G
gnomAD v4:
chr8-11486171-A-G
Joint Max Group AF
0.8572914 (AMR)
Genomes Max Group AF
0.8572914 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2254546
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11486171A>G , CM000670.2:g.11486171A>G
GRCh38
NC_000008.10:g.11343680A>G , CM000670.1:g.11343680A>G
GRCh37
NC_000008.9:g.11381089A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'