ClinGen Allele Registry
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Canonical Allele Identifier:
CA12866764
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.100795923A>C
GRCh37
chr8:g.101808151A>C
Linked Data - Sequence & Population
gnomAD v2:
8:101808151 A / C
gnomAD v3:
8:100795923 A / C
gnomAD v4:
chr8-100795923-A-C
Joint Max Group AF
0.30327681 (EAS)
Genomes Max Group AF
0.30327681 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10464815
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.100795923A>C , CM000670.2:g.100795923A>C
GRCh38
NC_000008.10:g.101808151A>C , CM000670.1:g.101808151A>C
GRCh37
NC_000008.9:g.101877327A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'