ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14799002
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.46132846T>G
GRCh37
chr20:g.44761485T>G
Linked Data - Sequence & Population
gnomAD v2:
20:44761485 T / G
gnomAD v3:
20:46132846 T / G
gnomAD v4:
chr20-46132846-T-G
Joint Max Group AF
0.44131977 (EAS)
Genomes Max Group AF
0.44131977 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12480534
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46132846T>G , CM000682.2:g.46132846T>G
GRCh38
NC_000020.10:g.44761485T>G , CM000682.1:g.44761485T>G
GRCh37
NC_000020.9:g.44194892T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'