ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13427602
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.102875061T>C
GRCh37
chr11:g.102745791T>C
Linked Data - Sequence & Population
gnomAD v2:
11:102745791 T / C
gnomAD v3:
11:102875061 T / C
gnomAD v4:
chr11-102875061-T-C
Joint Max Group AF
0.12754929 (NFE)
Genomes Max Group AF
0.1262029 (NFE)
Exomes Max Group AF
0.12745625 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2276109
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.102875061T>C , CM000673.2:g.102875061T>C
GRCh38
NC_000011.9:g.102745791T>C , CM000673.1:g.102745791T>C
GRCh37
NC_000011.8:g.102251001T>C
NCBI36
NG_032936.1:g.4974A>G
Search 100 bp 5'
Search 100 bp 3'