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Canonical Allele Identifier:
CA15682931
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.109022119C>T
GRCh37
chr11:g.108892846C>T
Linked Data - Sequence & Population
gnomAD v2:
11:108892846 C / T
gnomAD v3:
11:109022119 C / T
gnomAD v4:
chr11-109022119-C-T
Joint Max Group AF
0.26327738 (EAS)
Genomes Max Group AF
0.26327738 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4754373
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.109022119C>T , CM000673.2:g.109022119C>T
GRCh38
NC_000011.9:g.108892846C>T , CM000673.1:g.108892846C>T
GRCh37
NC_000011.8:g.108398056C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'