ClinGen Allele Registry
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Canonical Allele Identifier:
CA10664572
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22665150C>G
GRCh37
chr1:g.22991643C>G
Linked Data - Sequence & Population
gnomAD v2:
1:22991643 C / G
gnomAD v3:
1:22665150 C / G
gnomAD v4:
chr1-22665150-C-G
Joint Max Group AF
0.6636213 (AFR)
Genomes Max Group AF
0.6636213 (AFR)
Linked Data - NCBI & NCI
dbSNP:
647955
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22665150C>G , CM000663.2:g.22665150C>G
GRCh38
NC_000001.10:g.22991643C>G , CM000663.1:g.22991643C>G
GRCh37
NC_000001.9:g.22864230C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'