ClinGen Allele Registry
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Canonical Allele Identifier:
CA13172349
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.123121986T>C
GRCh37
chr10:g.124881502T>C
Linked Data - Sequence & Population
gnomAD v2:
10:124881502 T / C
gnomAD v3:
10:123121986 T / C
gnomAD v4:
chr10-123121986-T-C
Joint Max Group AF
0.83752058 (EAS)
Genomes Max Group AF
0.83752058 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10794595
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.123121986T>C , CM000672.2:g.123121986T>C
GRCh38
NC_000010.10:g.124881502T>C , CM000672.1:g.124881502T>C
GRCh37
NC_000010.9:g.124871492T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'