ClinGen Allele Registry
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Canonical Allele Identifier:
CA12898881
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.116635549G>A
GRCh37
chr8:g.117647788G>A
Linked Data - Sequence & Population
gnomAD v2:
8:117647788 G / A
gnomAD v3:
8:116635549 G / A
gnomAD v4:
chr8-116635549-G-A
Joint Max Group AF
0.87740606 (NFE)
Genomes Max Group AF
0.87740606 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6469656
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.116635549G>A , CM000670.2:g.116635549G>A
GRCh38
NC_000008.10:g.117647788G>A , CM000670.1:g.117647788G>A
GRCh37
NC_000008.9:g.117716969G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'