ClinGen Allele Registry
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Canonical Allele Identifier:
CA173622589
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.19994799C>G
GRCh37
chr8:g.19852310C>G
Linked Data - Sequence & Population
gnomAD v2:
8:19852310 C / G
gnomAD v3:
8:19994799 C / G
gnomAD v4:
chr8-19994799-C-G
Joint Max Group AF
0.26413921 (NFE)
Genomes Max Group AF
0.26413921 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17411031
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.19994799C>G , CM000670.2:g.19994799C>G
GRCh38
NC_000008.10:g.19852310C>G , CM000670.1:g.19852310C>G
GRCh37
NC_000008.9:g.19896590C>G
NCBI36
Search 100 bp 5'
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