ClinGen Allele Registry
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Canonical Allele Identifier:
CA845637882
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.11204283C>A
GRCh37
chr8:g.11061792C>A
Linked Data - Sequence & Population
gnomAD v3:
8:11204283 C / A
gnomAD v4:
chr8-11204283-C-A
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6981523
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11204283C>A , CM000670.2:g.11204283C>A
GRCh38
NC_000008.10:g.11061792C>A , CM000670.1:g.11061792C>A
GRCh37
NC_000008.9:g.11099202C>A
NCBI36
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