ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13201000
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99531836T>C
GRCh37
chr10:g.101291593T>C
Linked Data - Sequence & Population
gnomAD v2:
10:101291593 T / C
gnomAD v3:
10:99531836 T / C
gnomAD v4:
chr10-99531836-T-C
Joint Max Group AF
0.60984666 (AFR)
Genomes Max Group AF
0.60984666 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11190140
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99531836T>C , CM000672.2:g.99531836T>C
GRCh38
NC_000010.10:g.101291593T>C , CM000672.1:g.101291593T>C
GRCh37
NC_000010.9:g.101281583T>C
NCBI36
NG_016854.1:g.3904T>C
Search 100 bp 5'
Search 100 bp 3'