ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA226954558
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.92958366T>C
GRCh37
chr11:g.92691532T>C
Linked Data - Sequence & Population
gnomAD v2:
11:92691532 T / C
gnomAD v3:
11:92958366 T / C
gnomAD v4:
chr11-92958366-T-C
Joint Max Group AF
0.63871789 (AFR)
Genomes Max Group AF
0.63871789 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2166706
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.92958366T>C , CM000673.2:g.92958366T>C
GRCh38
NC_000011.9:g.92691532T>C , CM000673.1:g.92691532T>C
GRCh37
NC_000011.8:g.92331180T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'