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Canonical Allele Identifier:
CA14826102
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.6999988G>T
GRCh37
chr20:g.6980635G>T
Linked Data - Sequence & Population
gnomAD v2:
20:6980635 G / T
gnomAD v3:
20:6999988 G / T
gnomAD v4:
chr20-6999988-G-T
Joint Max Group AF
0.05805765 (NFE)
Genomes Max Group AF
0.05805765 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6085820
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.6999988G>T , CM000682.2:g.6999988G>T
GRCh38
NC_000020.10:g.6980635G>T , CM000682.1:g.6980635G>T
GRCh37
NC_000020.9:g.6928635G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'