ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13163965
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.89058620T>C
GRCh37
chr10:g.90818377T>C
Linked Data - Sequence & Population
gnomAD v2:
10:90818377 T / C
gnomAD v3:
10:89058620 T / C
gnomAD v4:
chr10-89058620-T-C
Joint Max Group AF
0.50332952 (AFR)
Genomes Max Group AF
0.50332952 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7920888
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.89058620T>C , CM000672.2:g.89058620T>C
GRCh38
NC_000010.10:g.90818377T>C , CM000672.1:g.90818377T>C
GRCh37
NC_000010.9:g.90808357T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'