ClinGen Allele Registry
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Canonical Allele Identifier:
CA12926320
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.19793650T>C
GRCh37
chr8:g.19651161T>C
Linked Data - Sequence & Population
gnomAD v2:
8:19651161 T / C
gnomAD v3:
8:19793650 T / C
gnomAD v4:
chr8-19793650-T-C
Joint Max Group AF
0.49029717 (SAS)
Genomes Max Group AF
0.49029717 (SAS)
Linked Data - NCBI & NCI
dbSNP:
920590
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.19793650T>C , CM000670.2:g.19793650T>C
GRCh38
NC_000008.10:g.19651161T>C , CM000670.1:g.19651161T>C
GRCh37
NC_000008.9:g.19695441T>C
NCBI36
Search 100 bp 5'
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