ClinGen Allele Registry
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Canonical Allele Identifier:
CA311592096
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.7771719C>T
GRCh37
chr20:g.7752366C>T
Linked Data - Sequence & Population
gnomAD v2:
20:7752366 C / T
gnomAD v3:
20:7771719 C / T
gnomAD v4:
chr20-7771719-C-T
Joint Max Group AF
0.29530456 (SAS)
Genomes Max Group AF
0.29530456 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6077251
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.7771719C>T , CM000682.2:g.7771719C>T
GRCh38
NC_000020.10:g.7752366C>T , CM000682.1:g.7752366C>T
GRCh37
NC_000020.9:g.7700366C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'