ClinGen Allele Registry
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Canonical Allele Identifier:
CA14754802
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.31431051C>T
GRCh37
chr20:g.30018854C>T
Linked Data - Sequence & Population
gnomAD v2:
20:30018854 C / T
gnomAD v3:
20:31431051 C / T
gnomAD v4:
chr20-31431051-C-T
Joint Max Group AF
0.71937953 (EAS)
Genomes Max Group AF
0.71937953 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2180566
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.31431051C>T , CM000682.2:g.31431051C>T
GRCh38
NC_000020.10:g.30018854C>T , CM000682.1:g.30018854C>T
GRCh37
NC_000020.9:g.29482515C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'