ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14783402
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.6718948T>G
GRCh37
chr20:g.6699595T>G
Linked Data - Sequence & Population
gnomAD v2:
20:6699595 T / G
gnomAD v3:
20:6718948 T / G
gnomAD v4:
chr20-6718948-T-G
Joint Max Group AF
0.43058495 (SAS)
Genomes Max Group AF
0.43058495 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4813802
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.6718948T>G , CM000682.2:g.6718948T>G
GRCh38
NC_000020.10:g.6699595T>G , CM000682.1:g.6699595T>G
GRCh37
NC_000020.9:g.6647595T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'