ClinGen Allele Registry
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Canonical Allele Identifier:
CA11929539
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.56027067C>A
GRCh37
chr5:g.55322895C>A
Linked Data - Sequence & Population
gnomAD v2:
5:55322895 C / A
gnomAD v3:
5:56027067 C / A
gnomAD v4:
chr5-56027067-C-A
Joint Max Group AF
0.19909306 (SAS)
Genomes Max Group AF
0.19909306 (SAS)
Linked Data - NCBI & NCI
dbSNP:
17348299
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.56027067C>A , CM000667.2:g.56027067C>A
GRCh38
NC_000005.9:g.55322895C>A , CM000667.1:g.55322895C>A
GRCh37
NC_000005.8:g.55358652C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'