ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14853525
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.40056900C>T
GRCh37
chr20:g.38685541C>T
Linked Data - Sequence & Population
gnomAD v2:
20:38685541 C / T
gnomAD v3:
20:40056900 C / T
gnomAD v4:
chr20-40056900-C-T
Joint Max Group AF
0.25066771 (EAS)
Genomes Max Group AF
0.25066771 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2870137
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.40056900C>T , CM000682.2:g.40056900C>T
GRCh38
NC_000020.10:g.38685541C>T , CM000682.1:g.38685541C>T
GRCh37
NC_000020.9:g.38118955C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'