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Canonical Allele Identifier:
CA13384979
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.65726789G>T
GRCh37
chr11:g.65494260G>T
Linked Data - Sequence & Population
gnomAD v2:
11:65494260 G / T
gnomAD v3:
11:65726789 G / T
gnomAD v4:
chr11-65726789-G-T
Joint Max Group AF
0.59874391 (AMR)
Genomes Max Group AF
0.59647704 (AMR)
Exomes Max Group AF
0.60300234 (AMR)
Linked Data - NCBI & NCI
dbSNP:
478304
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.65726789G>T , CM000673.2:g.65726789G>T
GRCh38
NC_000011.9:g.65494260G>T , CM000673.1:g.65494260G>T
GRCh37
NC_000011.8:g.65250836G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'